Worldwide Study Finder

Phase not reported / not applicableUnknownOBSERVATIONAL

Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese

ClinicalTrials.gov · NCT02166437 · Registry updated: 2016-10-19

Condition / research focus: Osteoporosis
Sponsor: Tomidahama Hospital
Countries with listed sites: Japan
Registry dates and results: Start: 2013-11. Completion: 2018-11 (may be estimated). No results posted in this registry response.

Products and interventions (0)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Where the study takes place — 1 listed sites

Site status can differ from overall study status. This list includes all reported sites, even when your search specifies one location. Confirm availability and eligibility with the study team through the original record.

Tomidahama Hospital
Yokkaichi, Mie-ken, Japan
Site recruitment: Recruiting

Original record, eligibility, contacts and results →

Phase 1CompletedINTERVENTIONAL

A Study to Determine the Patient Preference Between Zosano Pharma Parathyroid Hormone (ZP-PTH) Patch and Forteo Pen

ClinicalTrials.gov · NCT02478879 · Registry updated: 2016-08-23

Condition / research focus: Postmenopausal Osteoporosis
Sponsor: Zosano Pharma Corporation
Countries with listed sites: United States
Registry dates and results: Start: 2015-06. Completion: 2015-12 (may be estimated). No results posted in this registry response.

Products and interventions (2)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

ZP-PTH (drug) — also listed as: PTH, parathyroid hormone, teriparatide
FORTEO (drug) — also listed as: PTH, FORSTEO, teriparatide

Where the study takes place — 1 listed sites

Covance Daytona Beach Clinical Research Unit
Daytona Beach, Florida, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 1CompletedINTERVENTIONAL

A Comparison Study of PF708 and Forteo in Healthy Subjects

ClinicalTrials.gov · NCT02656810 · Registry updated: 2016-08-04

Condition / research focus: Osteoporosis
Sponsor: Pfenex, Inc
Countries with listed sites: United States
Registry dates and results: Start: 2015-12. Completion: 2016-07 (may be estimated). No results posted in this registry response.

Products and interventions (1)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: PF708

Where the study takes place — 1 listed sites

Covance Clinical Research Unit
Evansville, Indiana, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 1CompletedINTERVENTIONAL

Clinical Study of AK159 in Healthy Postmenopausal Women

ClinicalTrials.gov · NCT01551602 · Registry updated: 2016-07-25

Condition / research focus: Osteoporosis
Sponsor: Asahi Kasei Therapeutics Corporation
Countries with listed sites: Japan
Registry dates and results: Start: 2012-03. Completion: 2012-10 (may be estimated). No results posted in this registry response.

Products and interventions (3)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

AK159 (drug)
MN-10-T (drug)
Placebo (drug)

Where the study takes place — 3 listed sites

Facility not reported
Fukuoka, Japan
Site recruitment: Not reported
Facility not reported
Kumamoto, Japan
Site recruitment: Not reported
Facility not reported
Tokyo, Japan
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2CompletedINTERVENTIONAL

Adding Phosphorus to Osteoporosis Drug Treatment

ClinicalTrials.gov · NCT00074711 · Registry updated: 2016-07-06

Condition / research focus: Osteoporosis; Osteopenia
Sponsor: Creighton University
Countries with listed sites: United States
Registry dates and results: Start: 2004-08. Completion: 2008-06 (may be estimated). Results are posted in this registry.

Products and interventions (2)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Calcium carbonate (drug)
Calcium Phosphate (drug)

Where the study takes place — 1 listed sites

Creighton University Medical Center
Omaha, Nebraska, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2CompletedINTERVENTIONAL

Comparison Study of PTHrP and PTH to Treat Osteoporosis

ClinicalTrials.gov · NCT00853723 · Registry updated: 2016-03-24

Condition / research focus: Osteoporosis
Sponsor: University of Pittsburgh
Countries with listed sites: United States
Registry dates and results: Start: 2009-05. Completion: 2012-06 (may be estimated). Results are posted in this registry.

Products and interventions (3)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Parathyroid hormone related protein (1-36) (drug) — also listed as: PTHrP (1-36), PTHrP
Parathyroid hormone related protein(1-36) (drug) — also listed as: PTHrP (1-36), PTHrP
Parathyroid hormone (1-34) (drug) — also listed as: PTH(1-34), Teriparatide (brand name: Forteo)

Where the study takes place — 1 listed sites

UPMC Clinical & Translational Research Center
Pittsburgh, Pennsylvania, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 4CompletedINTERVENTIONAL

Effects of Teriparatide or Denosumab on Bone in Postmenopausal Women With Osteoporosis

ClinicalTrials.gov · NCT01753856 · Registry updated: 2015-10-08

Condition / research focus: Osteoporosis
Sponsor: Eli Lilly and Company
Countries with listed sites: Canada · United States
Registry dates and results: Start: 2013-01. Completion: 2014-06 (may be estimated). Results are posted in this registry.

Products and interventions (6)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: LY333334, Forteo, Forsteo
Denosumab (drug)
Demeclocycline (drug)
Tetracycline (drug)
Calcium Supplement (drug)
Vitamin D (drug)

Where the study takes place — 6 listed sites

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Lakewood, Colorado, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Gainesville, Georgia, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Detroit, Michigan, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Omaha, Nebraska, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Vancouver, British Columbia, Canada
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Sainte-Foy, Quebec, Canada
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2CompletedINTERVENTIONAL

A Pilot Study to Assess the Safety and Efficacy of Oral PTH (1-34) in the Treatment of Hypoparathyroidism

ClinicalTrials.gov · NCT02152228 · Registry updated: 2015-10-07

Condition / research focus: Hypoparathyroidism
Sponsor: Entera Bio Ltd.
Countries with listed sites: Israel
Registry dates and results: Start: 2014-07. Completion: 2015-07 (may be estimated). No results posted in this registry response.

Products and interventions (1)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

EnteraBio's Oral Parathyroid Hormone (1-34) (drug) — also listed as: Teriparatide

Where the study takes place — 1 listed sites

Lin Medical Center
Haifa, Israel
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 1CompletedINTERVENTIONAL

A Three Stage, Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of Oral PTH (1-34) in Healthy Subjects

ClinicalTrials.gov · NCT02202603 · Registry updated: 2015-10-07

Condition / research focus: Drug Safety
Sponsor: Entera Bio Ltd.
Countries with listed sites: Israel
Registry dates and results: Start: 2011-07. Completion: 2013-08 (may be estimated). No results posted in this registry response.

Products and interventions (3)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug)
Teriparatide (drug)
placebo (drug)

Where the study takes place — 1 listed sites

HMO Clinical Research Center Hadassah Ein Kerem Medical Center
Jerusalem, Israel
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 4CompletedINTERVENTIONAL

Teriparatide Treatment in Patients With Inherited Osteoporosis

ClinicalTrials.gov · NCT01360424 · Registry updated: 2015-09-29

Condition / research focus: Osteoporosis
Sponsor: Helsinki University Central Hospital
Countries with listed sites: Finland
Registry dates and results: Start: 2011-05. Completion: 2013-11 (may be estimated). No results posted in this registry response.

Products and interventions (1)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug)

Where the study takes place — 1 listed sites

Department of Orthopaedics and Traumatology and Division of Endocrinology, Department of Medicine and Pediatric Endocrinology, Hospital for Children and Adolescents, Helsinki University Central Hospital
Helsinki, Finland
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 4SuspendedINTERVENTIONAL

Treatment of Atraumatic Bone Marrow Edema With Denosumab and Teriparatide vs Placebo

ClinicalTrials.gov · NCT01734824 · Registry updated: 2015-09-23

Condition / research focus: Bone Marrow Oedema Syndrome; High Turnover Bone Disease; Quality of Life
Sponsor: Medical University of Vienna
Countries with listed sites: Austria
Registry dates and results: Start: 2012-05. Completion: 2015-09 (may be estimated). No results posted in this registry response.

Products and interventions (4)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Denosumab (drug) — also listed as: Prolia
Teriparatide (drug) — also listed as: PTH 1-34
Placebo Denosumab (drug) — also listed as: Prolia
Placebo Teriparatide (drug) — also listed as: PTH 1-34

Where the study takes place — 1 listed sites

Medical University Vienna - St. Vincent Hospital
Vienna, State of Vienna, Austria
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 3WithdrawnINTERVENTIONAL

Teriparatide for Fracture Repair in Humans

ClinicalTrials.gov · NCT02091492 · Registry updated: 2015-09-17

Condition / research focus: Osteoporosis, Age-Related; Humeral Fractures
Sponsor: Medical University of Vienna
Countries with listed sites: Austria
Registry dates and results: Start: 2014-06. Completion: 2015-09 (may be estimated). No results posted in this registry response.

Products and interventions (2)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: Forteo
Placebo (drug)

Where the study takes place — 1 listed sites

Medical University Vienna; St. Vincent Hospital
Vienna, State of Vienna, Austria
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2CompletedINTERVENTIONAL

Parathyroid Hormone (PTH) With Alendronate for Osteoporosis

ClinicalTrials.gov · NCT00005006 · Registry updated: 2015-08-19

Condition / research focus: Osteoporosis
Sponsor: Helen Hayes Hospital
Countries with listed sites: United States
Registry dates and results: Start: 1987-09. Completion: 2006-12 (may be estimated). No results posted in this registry response.

Products and interventions (3)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Parathyroid Hormone (drug) — also listed as: Fosamax, Forteo
Alendronate (drug)
Teriparatide (drug)

Where the study takes place — 1 listed sites

Helen Hayes Hospital, Clinical Research Center
West Haverstraw, New York, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2 / Phase 3CompletedINTERVENTIONAL

Bone Properties in Hypoparathyroidism: Effects of PTH

ClinicalTrials.gov · NCT00473265 · Registry updated: 2015-07-16

Condition / research focus: Hypoparathyroidism
Sponsor: John P. Bilezikian
Countries with listed sites: United States
Registry dates and results: Start: 2004-05. Completion: 2014-06 (may be estimated). Results are posted in this registry.

Products and interventions (1)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

PTH (drug) — also listed as: teriparatide, Preotact, PTH1-84, rhPTH, Natpara

Where the study takes place — 1 listed sites

Columbia University
New York, New York, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 4CompletedINTERVENTIONAL

Risedronate and Parathyroid Hormone to Reverse Osteoporosis Caused by Chronic Steroid Use

ClinicalTrials.gov · NCT00221299 · Registry updated: 2015-06-25

Condition / research focus: Osteoporosis
Sponsor: University of California, Davis
Countries with listed sites: United States
Registry dates and results: Start: 2005-09. Completion: 2009-05 (may be estimated). Results are posted in this registry.

Products and interventions (2)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Risedronate (drug) — also listed as: Actonel, NDC# 0149-0472-04
Parathyroid Hormone (drug) — also listed as: Forteo, PTH, rhPTH 1-34, NDC# 0002-8971-01

Where the study takes place — 1 listed sites

UC Davis General Medicine Research Clinic
Sacramento, California, United States
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 3CompletedINTERVENTIONAL

Effect of Teriparatide on Hip Fracture Healing

ClinicalTrials.gov · NCT01473589 · Registry updated: 2015-04-16

Condition / research focus: Femur Neck Fracture
Sponsor: Eli Lilly and Company
Countries with listed sites: Australia · Canada · Denmark · Estonia · Finland · Hong Kong · India · Israel · Japan · Latvia · Lithuania · New Zealand · Norway · Puerto Rico · South Korea · Spain · Sweden · Taiwan · United States
Registry dates and results: Start: 2012-02. Completion: 2013-12 (may be estimated). Results are posted in this registry.

Products and interventions (4)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: Forteo, Forsteo, LY333334
Placebo (drug)
Calcium supplementation (dietary_supplement)
Vitamin D supplementation (dietary_supplement)

Where the study takes place — 92 listed sites

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Phoenix, Arizona, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Tucson, Arizona, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
La Mesa, California, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Laguna Hills, California, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Lancaster, California, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Pasadena, California, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Danbury, Connecticut, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Boca Raton, Florida, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Bradenton, Florida, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Miami, Florida, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Orlando, Florida, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Idaho Falls, Idaho, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Royal Oak, Michigan, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Columbia, Missouri, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Springfield, Missouri, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Billings, Montana, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Great Falls, Montana, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Omaha, Nebraska, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Asheville, North Carolina, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Fargo, North Dakota, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
York, Pennsylvania, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Houston, Texas, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
San Antonio, Texas, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Salt Lake City, Utah, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Penrith, New South Wales, Australia
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Heidelberg, Victoria, Australia
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
St Albans, Victoria, Australia
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Nedlands, Western Australia, Australia
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Newmarket, Ontario, Canada
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
St. Catharines, Ontario, Canada
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Saint-Jérôme, Quebec, Canada
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Aarhus, Denmark
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Copenhagen, Denmark
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Hillerød, Denmark
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Koege, Denmark
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Tartu, Estonia
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Oulu, Finland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Turku, Finland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Hong Kong, Hong Kong
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Ahmedabad, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Attavar, Mangalore, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Bangalore, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Hyderabaad, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Nagpur, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Vadodara, India
Site recruitment: Not reported
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Haifa, Israel
Site recruitment: Not reported
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Jerusalem, Israel
Site recruitment: Not reported
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Aichi, Japan
Site recruitment: Not reported
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Chiba, Japan
Site recruitment: Not reported
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Fukuoka, Japan
Site recruitment: Not reported
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Fukushima, Japan
Site recruitment: Not reported
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Gunma, Japan
Site recruitment: Not reported
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Hiroshima, Japan
Site recruitment: Not reported
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Ibaraki, Japan
Site recruitment: Not reported
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Japan, Japan
Site recruitment: Not reported
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Kagawa, Japan
Site recruitment: Not reported
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Nagano, Japan
Site recruitment: Not reported
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Niigata, Japan
Site recruitment: Not reported
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Ohita, Japan
Site recruitment: Not reported
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Osaka, Japan
Site recruitment: Not reported
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Saga, Japan
Site recruitment: Not reported
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Shimane, Japan
Site recruitment: Not reported
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Shizuoka, Japan
Site recruitment: Not reported
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Toyama, Japan
Site recruitment: Not reported
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Toyko, Japan
Site recruitment: Not reported
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Yamaguchi, Japan
Site recruitment: Not reported
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Yamanashi, Japan
Site recruitment: Not reported
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Riga, Latvia
Site recruitment: Not reported
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Kaunas, Lithuania
Site recruitment: Not reported
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Klaipėda, Lithuania
Site recruitment: Not reported
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Vilnius, Lithuania
Site recruitment: Not reported
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Christchurch, New Zealand
Site recruitment: Not reported
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Takapuna, New Zealand
Site recruitment: Not reported
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Wellington South, New Zealand
Site recruitment: Not reported
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Tønsberg, Norway
Site recruitment: Not reported
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San Juan, Puerto Rico
Site recruitment: Not reported
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Seongnam-si, South Korea
Site recruitment: Not reported
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Seoul, South Korea
Site recruitment: Not reported
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Alzira, Spain
Site recruitment: Not reported
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Barcelona, Spain
Site recruitment: Not reported
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Girona, Spain
Site recruitment: Not reported
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Guadalajara, Spain
Site recruitment: Not reported
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Marbella, Spain
Site recruitment: Not reported
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Pozuelo de Alarcón, Spain
Site recruitment: Not reported
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Malmö, Sweden
Site recruitment: Not reported
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Mölndal, Sweden
Site recruitment: Not reported
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Stockholm, Sweden
Site recruitment: Not reported
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Kaohsiung City, Taiwan
Site recruitment: Not reported
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Taichung, Taiwan
Site recruitment: Not reported
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Taichung, Taiwan
Site recruitment: Not reported
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Taipei, Taiwan
Site recruitment: Not reported
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Zhonghe, Taiwan
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 3CompletedINTERVENTIONAL

Second Study of the Effect of Teriparatide on Hip Fracture Healing

ClinicalTrials.gov · NCT01473602 · Registry updated: 2015-04-16

Condition / research focus: Femur Neck Fracture
Sponsor: Eli Lilly and Company
Countries with listed sites: Belgium · Croatia · France · Germany · Greece · Hungary · India · Netherlands · Poland · Romania · South Korea · Switzerland · Turkey (Türkiye) · United States
Registry dates and results: Start: 2012-01. Completion: 2013-11 (may be estimated). Results are posted in this registry.

Products and interventions (4)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: Forteo, Forsteo, LY333334
Placebo (drug)
Calcium supplementation (dietary_supplement)
Vitamin D supplementation (dietary_supplement)

Where the study takes place — 75 listed sites

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
San Diego, California, United States
Site recruitment: Not reported
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Golden, Colorado, United States
Site recruitment: Not reported
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Washington D.C., District of Columbia, United States
Site recruitment: Not reported
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Gainesville, Georgia, United States
Site recruitment: Not reported
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Morton Grove, Illinois, United States
Site recruitment: Not reported
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Rockford, Illinois, United States
Site recruitment: Not reported
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Indianapolis, Indiana, United States
Site recruitment: Not reported
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Detroit, Michigan, United States
Site recruitment: Not reported
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New Hyde Park, New York, United States
Site recruitment: Not reported
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New York, New York, United States
Site recruitment: Not reported
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Charlotte, North Carolina, United States
Site recruitment: Not reported
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Durham, North Carolina, United States
Site recruitment: Not reported
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Danville, Pennsylvania, United States
Site recruitment: Not reported
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Pittsburgh, Pennsylvania, United States
Site recruitment: Not reported
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Charleston, South Carolina, United States
Site recruitment: Not reported
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Johnson City, Tennessee, United States
Site recruitment: Not reported
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Memphis, Tennessee, United States
Site recruitment: Not reported
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Charlottesville, Virginia, United States
Site recruitment: Not reported
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Falls Church, Virginia, United States
Site recruitment: Not reported
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Aalst, Belgium
Site recruitment: Not reported
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Blankenberge, Belgium
Site recruitment: Not reported
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Brussels, Belgium
Site recruitment: Not reported
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Genk, Belgium
Site recruitment: Not reported
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Gilly, Belgium
Site recruitment: Not reported
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Leuven, Belgium
Site recruitment: Not reported
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Osijek, Croatia
Site recruitment: Not reported
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Rijeka, Croatia
Site recruitment: Not reported
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Sisak, Croatia
Site recruitment: Not reported
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Slavonski Brod, Croatia
Site recruitment: Not reported
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Zagreb, Croatia
Site recruitment: Not reported
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La Roche-sur-Yon, France
Site recruitment: Not reported
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Orléans, France
Site recruitment: Not reported
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Saint-Etienne, France
Site recruitment: Not reported
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Toulouse, France
Site recruitment: Not reported
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Berlin, Germany
Site recruitment: Not reported
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Cologne, Germany
Site recruitment: Not reported
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Dresden, Germany
Site recruitment: Not reported
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Freiburg im Breisgau, Germany
Site recruitment: Not reported
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Göttingen, Germany
Site recruitment: Not reported
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Hamburg, Germany
Site recruitment: Not reported
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Leipzig, Germany
Site recruitment: Not reported
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Marburg, Germany
Site recruitment: Not reported
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Regensburg, Germany
Site recruitment: Not reported
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Haidari/Athens, Greece
Site recruitment: Not reported
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Kifissia, Greece
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Pátrai, Greece
Site recruitment: Not reported
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Thessaloniki, Greece
Site recruitment: Not reported
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Budapest, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Eger, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Hatvan, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Kaposvár, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Sopron, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Szeged, Hungary
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Attavar, Mangalore, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Bangalore, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Hyderabaad, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
New Delhi, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Pune, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Trivandrum, India
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Maastricht, Netherlands
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Zwolle, Netherlands
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Lublin, Poland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Warsaw, Poland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Bucharest, Romania
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Cluj-Napoca, Romania
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Timișoara, Romania
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Busan, South Korea
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Daegu, South Korea
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Seoul, South Korea
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Suwon, South Korea
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Basel, Switzerland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Lausanne, Switzerland
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Ankara, Turkey (Türkiye)
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Istanbul, Turkey (Türkiye)
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Izmir, Turkey (Türkiye)
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 4CompletedINTERVENTIONAL

The Forteo Alendronate Comparator Trial

ClinicalTrials.gov · NCT02416271 · Registry updated: 2015-04-14

Condition / research focus: Osteoporosis
Sponsor: Eli Lilly and Company
Countries with listed sites: Brazil · Mexico · Puerto Rico · United States
Registry dates and results: Start: 2001-04. Completion: 2003-05 (may be estimated). No results posted in this registry response.

Products and interventions (6)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

Teriparatide (drug) — also listed as: LY333334, Forteo, Forsteo
Alendronate (drug)
Calcium (dietary_supplement)
Vitamin D (dietary_supplement)
Placebo-Oral (drug)
Placebo-SC (drug)

Where the study takes place — 20 listed sites

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mobile, Alabama, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Tustin, California, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Lakewood, Colorado, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Honolulu, Hawaii, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Chicago, Illinois, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Springfield, Illinois, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Indianapolis, Indiana, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
West Boylston, Massachusetts, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Arden Hills, Minnesota, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
St Louis, Missouri, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Morristown, New Jersey, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Greenville, North Carolina, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Portland, Oregon, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Pittsburgh, Pennsylvania, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Providence, Rhode Island, United States
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Recife, Brazil
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
São Paulo, Brazil
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mexico City, Mexico
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mezzanine, Mexico
Site recruitment: Not reported
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
San Juan, Puerto Rico
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 2WithdrawnINTERVENTIONAL

Effect of PTH(1-34) Treatment on Fracture Healing in Vivo

ClinicalTrials.gov · NCT00741182 · Registry updated: 2015-03-18

Condition / research focus: Shoulder Fractures; Trochanteric Fractures
Sponsor: Glostrup University Hospital, Copenhagen
Countries with listed sites: Denmark
Registry dates and results: Start: 2008-10. Completion: 2010-09 (may be estimated). No results posted in this registry response.

Products and interventions (1)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

rhPTH(1-34) (drug) — also listed as: Forsteo, Forteo, Teriparatide

Where the study takes place — 1 listed sites

Research Center for Ageing and Osteoporosis, Glostrup University Hospital
Copenhagen, Denmark
Site recruitment: Not reported

Original record, eligibility, contacts and results →

Phase 1CompletedINTERVENTIONAL

A Study Aimed at Assessing the Pharmacokinetic Properties of RGB-10 and Forsteo

ClinicalTrials.gov · NCT02223416 · Registry updated: 2015-03-18

Condition / research focus: Healthy
Sponsor: Gedeon Richter Plc.
Countries with listed sites: United Kingdom
Registry dates and results: Start: Not reported. Completion: Not reported (may be estimated). No results posted in this registry response.

Products and interventions (2)

Includes comparators and combinations. A search match is not a verified peptide identity or evidence of benefit.

RGB-10 (drug)
Teriparatide (drug)

Where the study takes place — 1 listed sites

Celerion (UK)
Belfast, United Kingdom
Site recruitment: Not reported

Original record, eligibility, contacts and results →

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Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese

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A Study to Determine the Patient Preference Between Zosano Pharma Parathyroid Hormone (ZP-PTH) Patch and Forteo Pen

A Comparison Study of PF708 and Forteo in Healthy Subjects

Clinical Study of AK159 in Healthy Postmenopausal Women

Adding Phosphorus to Osteoporosis Drug Treatment

Comparison Study of PTHrP and PTH to Treat Osteoporosis

Effects of Teriparatide or Denosumab on Bone in Postmenopausal Women With Osteoporosis

A Pilot Study to Assess the Safety and Efficacy of Oral PTH (1-34) in the Treatment of Hypoparathyroidism

A Three Stage, Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of Oral PTH (1-34) in Healthy Subjects

Teriparatide Treatment in Patients With Inherited Osteoporosis

Treatment of Atraumatic Bone Marrow Edema With Denosumab and Teriparatide vs Placebo

Teriparatide for Fracture Repair in Humans

Parathyroid Hormone (PTH) With Alendronate for Osteoporosis

Bone Properties in Hypoparathyroidism: Effects of PTH

Risedronate and Parathyroid Hormone to Reverse Osteoporosis Caused by Chronic Steroid Use

Effect of Teriparatide on Hip Fracture Healing

Second Study of the Effect of Teriparatide on Hip Fracture Healing

The Forteo Alendronate Comparator Trial

Effect of PTH(1-34) Treatment on Fracture Healing in Vivo

A Study Aimed at Assessing the Pharmacokinetic Properties of RGB-10 and Forsteo

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