Paltusotine + Placebo
Phase 2Completed 0 watching 0 views this week⚡ Active
47
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Acromegaly
Conditions
Acromegaly
Trial Timeline
Mar 11, 2019 → Aug 12, 2020
NCT ID
NCT03792555About Paltusotine + Placebo
Paltusotine + Placebo is a phase 2 stage product being developed by Crinetics Pharmaceuticals for Acromegaly. The current trial status is completed. This product is registered under clinical trial identifier NCT03792555. Target conditions include Acromegaly.
Hype Score Breakdown
Clinical
17
Activity
12
Company
5
Novelty
5
Community
5
Clinical Trials (4)
| NCT ID | Phase | Status |
|---|---|---|
| NCT07087054 | Phase 3 | Recruiting |
| NCT05192382 | Phase 3 | Active |
| NCT04837040 | Phase 3 | Active |
| NCT03792555 | Phase 2 | Completed |
Competing Products
20 competing products in Acromegaly
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Alesse | Novartis | Phase 2 | 52 |
| ONO-5788 + ONO-5788 Placebo + Octreotide | Ono Pharmaceutical | Phase 1 | 33 |
| ONO-5788 + [14C]-ONO-5788 | Ono Pharmaceutical | Phase 1 | 33 |
| Pasireotide LAR | Novartis | Phase 3 | 77 |
| Octreotide acetate 30 mg suspension | Novartis | Phase 3 | 77 |
| Pasireotide long acting release formulation | Novartis | Pre-clinical | 23 |
| Sandostatin LAR + pegvisomant + cabergoline | Novartis | Approved | 85 |
| Octreotide acetate and cabergoline/Octrotide and Somavert | Novartis | Approved | 85 |
| Sandostatin LAR | Novartis | Approved | 85 |
| Pasireotide + Octreotide | Novartis | Phase 3 | 77 |
| Sandostatin (Octreotide Acetate) | Novartis | Approved | 85 |
| Octreotide acetate | Novartis | Approved | 85 |
| octreotide FluidCrystal® injection depot | Novartis | Phase 2 | 52 |
| Octreotide LAR | Novartis | Phase 3 | 77 |
| Octreotide LAR | Novartis | Phase 3 | 77 |
| Pasireotide | Novartis | Phase 2 | 52 |
| Pasireotide LAR 60 mg + Pegvisomant | Novartis | Approved | 85 |
| Octreotide | Novartis | Approved | 85 |
| Octreotide LAR 30 MG Injection | Novartis | Approved | 85 |
| Pasireotide LAR | Novartis | Phase 2 | 52 |