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DEPREOTIDE
DEPREOTIDE is a depreotide drug. It is currently in Phase 2 development.
Depreotide works by binding to a specific target, although its exact mechanism of action is unknown.
Depreotide is a protein modality. It has been studied in clinical trials for various conditions, including knee osteoarthritis, shoulder pain, and hemiplegia, in combination with platelet-rich plasma treatment or hyaluronic acid treatment.
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Baseline phase 2 → approval rate
+15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2031–2034 | — |
| EMA | EU | 2032–2035 | +0.7 yr |
| MHRA | GB | 2032–2035 | +0.7 yr |
| Health Canada | CA | 2032–2036 | +0.9 yr |
| TGA | AU | 2032–2036 | +1.2 yr |
| PMDA | JP | 2032–2036 | +1.5 yr |
| NMPA | CN | 2033–2037 | +2.3 yr |
| MFDS | KR | 2032–2036 | +1.4 yr |
| CDSCO | IN | 2032–2037 | +1.8 yr |
| ANVISA | BR | 2033–2037 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | DEPREOTIDE |
|---|---|
| Drug class | depreotide |
| Modality | Recombinant protein |
| Therapeutic area | Other |
| Phase | Phase 2 |
Mechanism of action
Think of depreotide like a key that fits into a lock. When it binds to its target, it can help to turn off or reduce the activity of certain processes in the body. This can help to treat conditions where these processes are overactive or problematic.
Approved indications
Common side effects
Key clinical trials
- Knee Osteoarthritis: Platelet Rich Plasma or Hyaluronic Acid (NA)
- Efficacy Of Platelet Rich Plasma In The Treatment Of Hemiplegıc Shoulder Pain (NA)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- DEPREOTIDE CI brief — competitive landscape report
- DEPREOTIDE updates RSS · CI watch RSS
Frequently asked questions about DEPREOTIDE
What is DEPREOTIDE?
How does DEPREOTIDE work?
What drug class is DEPREOTIDE in?
What development phase is DEPREOTIDE in?
Related
- Drug class: All depreotide drugs
- Therapeutic area: All drugs in Other
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing