Forteo® (teriparatide [rDNA origin] injection)

Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.

Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.

The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.

Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.

Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.

Clinical studies on Lilly products may also be sponsored and reported by parties other than Lilly in other clinical trial registries.

Trial Results

The following trials have been conducted for Forteo.

Disease Trial ID Trial Title Trial
Phase
Osteoporosis
8175
The Effect of Teriparatide on Distal Radius Fracture Healing
2
Osteoporosis
8464
Assessment of Dose Response of LY333334 in Japanese Postmenopausal Women with Osteoporosis
2
Osteoporosis
547
Effects of LY333334 in the Treatment of Postmenopausal Women with Osteoporosis
3
Osteoporosis 550
Effects of LY333334 in the Treatment of Men with Osteoporosis
3
Osteoporosis
6680
Comparison of Teriparatide and Calcitonin in the Treatment of Postmenopausal Women with Osteoporosis
3
Osteoporosis
8736
Efficacy and Safety of Teriparatide 20 µg in the Treatment of Postmenopausal Women with Osteoporosis
3
Osteoporosis
9151
TUHRS Study - Teriparatide Use in Hip Replaced Subjects. A Pilot Study on the Use of Teriparatide in Severe Osteoporotic Women with Hip Fracture and Submitted to Hip Replacement
3
Osteoporosis
6817
Combined Use of Teriparatide and Raloxifene in Postmenopausal Women with Osteoporosis
3b
Osteoporosis
8370
Compliance With and Acceptance of Teriparatide Pen Injection in Severely Osteoporotic Patients [CATS]
3b
Osteoporosis
6537
Comparison of a 2-Year Therapy of Teriparatide Alone and its Sequential Use for 1 Year, with or without Raloxifene HCl, in the Treatment of Severe Postmenopausal Osteoporosis
3 / 4
Osteoporosis
6972
Comparison of Teriparatide and Calcitonin in the Treatment of Postmenopausal Women with Osteoporosis
3 / 4
Osteoporosis
7918
Bone Effects of Subcutaneous Teriparatide Following Discontinuation of Alendronate Treatment in Postmenopausal Women With Osteoporosis
3 / 4
Osteoporosis
4943
Teriparatide Compared with Alendronate on Spine Bone Mineral Density in Postmenopausal Women with Osteoporosis
4
Osteoporosis
5490
Sequential Use of Teriparatide and Raloxifene HCl in the Treatment of Postmenopausal Women with Osteoporosis
4
Osteoporosis
5711
Bone Effects of Subcutaneous Teriparatide Following Discontinuation of Raloxifene or Alendronate Treatment in Postmenopausal Women with Osteoporosis
4
Osteoporosis
6573
Comparison of Teriparatide and Calcitonin in the Treatment of Postmenopausal Women with Osteoporosis
4
Osteoporosis
6715
Bone Marker Changes In One Month Treatment with Teriparatide (LY333334) Injections (rDNA Origin) in Men and Post Menopausal Women with Severe Osteoporosis
4
Osteoporosis
8141
Effects of Subcutaneous Teriparatide on Serum Calcium in Postmenopausal Women with Osteoporosis Previously Treated with Raloxifene or Alendronate
4
Osteoporosis
10080
Differential Effects of Teriparatide and Strontium Ranelate on Bone Remodeling and Formation in Postmenopausal Women with Osteoporosis: A Histomorphometric Study.
4