lanreotide (Autogel formulation) + Pegvisomant
Phase 3Completed 1 views this week 0 watching💤 Quiet
Interest: 37/100
37
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Acromegaly
Conditions
Acromegaly
Trial Timeline
Oct 1, 2006 → Oct 1, 2008
NCT ID
NCT00383708About lanreotide (Autogel formulation) + Pegvisomant
lanreotide (Autogel formulation) + Pegvisomant is a phase 3 stage product being developed by Ipsen for Acromegaly. The current trial status is completed. This product is registered under clinical trial identifier NCT00383708. Target conditions include Acromegaly.
What happened to similar drugs?
13 of 20 similar drugs in Acromegaly were approved
Approved (13) Terminated (1) Active (7)
Hype Score Breakdown
Clinical
17
Activity
8
Company
12
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00383708 | Phase 3 | Completed |
Competing Products
20 competing products in Acromegaly
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Alesse | Novartis | Phase 2 | 31 |
| ONO-5788 + ONO-5788 Placebo + Octreotide | Ono Pharmaceutical | Phase 1 | 21 |
| ONO-5788 + [14C]-ONO-5788 | Ono Pharmaceutical | Phase 1 | 29 |
| Pasireotide LAR | Novartis | Phase 3 | 40 |
| Octreotide acetate 30 mg suspension | Novartis | Phase 3 | 40 |
| Pasireotide long acting release formulation | Novartis | Pre-clinical | 26 |
| Sandostatin LAR + pegvisomant + cabergoline | Novartis | Approved | 43 |
| Octreotide acetate and cabergoline/Octrotide and Somavert | Novartis | Approved | 43 |
| Sandostatin LAR | Novartis | Approved | 43 |
| Pasireotide + Octreotide | Novartis | Phase 3 | 40 |
| Sandostatin (Octreotide Acetate) | Novartis | Approved | 39 |
| Octreotide acetate | Novartis | Approved | 35 |
| octreotide FluidCrystal® injection depot | Novartis | Phase 2 | 35 |
| Octreotide LAR | Novartis | Phase 3 | 40 |
| Octreotide LAR | Novartis | Phase 3 | 40 |
| Pasireotide | Novartis | Phase 2 | 35 |
| Pasireotide LAR 60 mg + Pegvisomant | Novartis | Approved | 39 |
| Octreotide | Novartis | Approved | 43 |
| Octreotide LAR 30 MG Injection | Novartis | Approved | 43 |
| Pasireotide LAR | Novartis | Phase 2 | 35 |