Trials / Completed
CompletedNCT01124006
A Multicenter, Randomized, Double-blind, Placebo Controlled, Clinical Trial to Evaluate the Safety, Tolerability and Preliminary Effectiveness of 2 Doses of Intradiscal rhGDF-5 (Single Administration) for the Treatment of Early Stage Lumbar Disc Degeneration
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 24 (actual)
- Sponsor
- DePuy Spine · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Study to show the safety and tolerability of Intradiscal rhGDF-5 in subjects with early lumbar disc degeneration
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intradiscal rhGDF-5 | The API is recombinant human growth and differentiation factor-5 (rhGDF-5), a recombinant version of human GDF-5. GDF-5 is a member of the transforming growth factor-b (TGF-b) superfamily and the bone morphogenetic protein (BMP) subfamily, and is known to influence the growth and differentiation of various tissues, including the intervertebral disc. In vitro experiments have shown that rhGDF-5 can stimulate gene expression and synthesis of the extracellular matrix proteins type II collagen and aggrecan. In vivo experiments in rabbit models of disc degeneration have shown that intradiscal injections of rhGDF-5 can stimulate an increase in disc height and hydration. |
| OTHER | Water for injection | Sterile water for injection |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2014-09-01
- Completion
- 2014-09-01
- First posted
- 2010-05-14
- Last updated
- 2016-02-24
- Results posted
- 2016-02-24
Locations
10 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01124006. Inclusion in this directory is not an endorsement.