Pasireotide LAR 60 mg + Pegvisomant
ApprovedUNKNOWN 0 views this week 0 watching💤 Quiet
Interest: 39/100
39
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Acromegaly
Conditions
Acromegaly
Trial Timeline
Aug 1, 2015 → Jun 1, 2017
NCT ID
NCT02668172About Pasireotide LAR 60 mg + Pegvisomant
Pasireotide LAR 60 mg + Pegvisomant is a approved stage product being developed by Novartis for Acromegaly. The current trial status is unknown. This product is registered under clinical trial identifier NCT02668172. Target conditions include Acromegaly.
What happened to similar drugs?
12 of 20 similar drugs in Acromegaly were approved
Approved (12) Terminated (1) Active (8)
Hype Score Breakdown
Clinical
20
Activity
4
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02668172 | Approved | UNKNOWN |
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 |
| Octreotide | Novartis | Approved | 43 |
| Octreotide LAR 30 MG Injection | Novartis | Approved | 43 |
| Pasireotide LAR | Novartis | Phase 2 | 35 |
| Pasireotide (SOM230), Octreotide (Sandostatin) | Novartis | Phase 2 | 35 |