Last reviewed · How we verify
NCT01124006
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
Phase 2 trial testing Intradiscal rhGDF-5 in Degenerative Disc Disease in 24 participants. Completed in 1 September 2014.
1 September 2014
Quick facts
| Lead sponsor | DePuy Spine |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 24 |
| Start date | 1 January 2010 |
| Primary completion | 1 September 2014 |
| Estimated completion | 1 September 2014 |
| Sites | 10 locations across United States |
Drugs / interventions tested
- Intradiscal rhGDF-5 — full drug profile →
- Water for injection — full drug profile →
Conditions studied
- Degenerative Disc Disease — all drugs for Degenerative Disc Disease →
Sponsor
DePuy Spine — full company profile →
Who can join
18 and older, any sex, with Degenerative Disc Disease. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Neurological Assessment for Motor Function and Reflexes/Sensory
Time frame: 12 months
Neurological Assessment for Motor Function and Reflexes/Sensory- Number of patients with Clinically Significant Abnormal results at 12 months. For Motor Function, Clinically Significant Abnormal results are determined by the surgeon investigator and are further classified by grade: 0= No Movement, 1= Flicker/trace of contraction, 2=Active movement when gravity removed, 3= Active movement against -
Treatment Emergent Adverse Events- Relationship to Study Drug
Time frame: Through a 12 month period and annual telephone contact at 24 and 36 months for subject health status follow-up.
Number of patients with Treatment Emergent Adverse Events that were designated as Definitely Related to Study Drug. -
Treatment Emergent Adverse Events- Relationship to Study Drug
Time frame: 12 month period and annual telephone contact at 24 and 36 months for subject health status follow-up
Number of patients with Treatment Emergent Adverse Events that were designated as Possibly or Probably Related to Study Drug.
Sponsor's own description
Study to show the safety and tolerability of Intradiscal rhGDF-5 in subjects with early lumbar disc degeneration
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Stem Cells and Exosomes: New Therapies for Intervertebral Disc Degeneration.
Krut Z, Pelled G, Gazit D, Gazit Z. · · 2021 · cited 129× · PMID 34571890 · DOI 10.3390/cells10092241 -
Intervertebral Disc Degeneration: Biomaterials and Tissue Engineering Strategies toward Precision Medicine.
Mohd Isa IL, Mokhtar SA, Abbah SA, Fauzi MB, et al · · 2022 · cited 101× · PMID 35373924 · DOI 10.1002/adhm.202102530 -
Intervertebral disc degeneration-Current therapeutic options and challenges.
Samanta A, Lufkin T, Kraus P. · · 2023 · cited 98× · PMID 37483952 · DOI 10.3389/fpubh.2023.1156749 -
Strategies for Annulus Fibrosus Regeneration: From Biological Therapies to Tissue Engineering.
Chu G, Shi C, Wang H, Zhang W, et al · · 2018 · cited 76× · PMID 30042942 · DOI 10.3389/fbioe.2018.00090 -
Intervertebral Disc Nucleus Repair: Hype or Hope?
Tendulkar G, Chen T, Ehnert S, Kaps HP, et al · · 2019 · cited 54× · PMID 31344903 · DOI 10.3390/ijms20153622 -
Potential regenerative treatment strategies for intervertebral disc degeneration in dogs.
Bach FC, Willems N, Penning LC, Ito K, et al · · 2014 · cited 46× · PMID 24387033 · DOI 10.1186/1746-6148-10-3 -
Leaping the hurdles in developing regenerative treatments for the intervertebral disc from preclinical to clinical.
Thorpe AA, Bach FC, Tryfonidou MA, Le Maitre CL, et al · · 2018 · cited 43× · PMID 31463447 · DOI 10.1002/jsp2.1027 -
Development, Pathogenesis, and Regeneration of the Intervertebral Disc: Current and Future Insights Spanning Traditional to Omics Methods.
Hickman TT, Rathan-Kumar S, Peck SH. · · 2022 · cited 40× · PMID 35359439 · DOI 10.3389/fcell.2022.841831
Verify or expand the search:
- PubMed search for NCT01124006
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Degenerative Disc Disease
Currently open trials in the same condition.
- NCT07254806 — A Study to Evaluate the Effectiveness of IDCT (Intradiscal Cell Therapy) in Subjects With One Level, Symptomatic Mild to · Phase 3 · recruiting
- NCT04679844 — Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Au · NA · recruiting
- NCT06704919 — Conduit Cages and Fibergraft BG Putty · recruiting
- NCT06053242 — Safety, Tolerability, and Effectiveness of Intramuscular Injection of CELZ-201-DDT for the Treatment of Chronic Lower Ba · Phase 1, PHASE2 · recruiting
- NCT03810573 — Evaluation of NB1 Bone Graft Following Lumbar Interbody Arthrodesis · NA · recruiting
Other DePuy Spine trials
Trials by the same sponsor.
- NCT02814825 — An ACDF Multi-Center Study Using ViviGen Cellular Bone Matrix · completed
- NCT00432159 — Comparison of DISCOVER™ Artificial Cervical Disc and ACDF for Treatment of Cervical DDD (IDE Study) · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT01124006 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by DePuy Spine
- Last refreshed: 26 January 2016
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01124006.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing