Somatropin (recombinant deoxyribonucleic acid [rDNA] origin)
Pre-clinicalCompletedDevelopment Stage
Growth Hormone (GH) Deficiency
Growth Hormone (GH) Deficiency, Short Stature Homeobox Containing Gene (SHOX) Deficiency, SHOX Deficiency-related Disorder, Non-GH-deficient Growth Disorders
Apr 1, 1999 → Sep 1, 2015
About Somatropin (recombinant deoxyribonucleic acid [rDNA] origin)
Somatropin (recombinant deoxyribonucleic acid [rDNA] origin) is a pre-clinical stage product being developed by Eli Lilly for Growth Hormone (GH) Deficiency. The current trial status is completed. This product is registered under clinical trial identifier NCT01088412. Target conditions include Growth Hormone (GH) Deficiency, Short Stature Homeobox Containing Gene (SHOX) Deficiency, SHOX Deficiency-related Disorder.
What happened to similar drugs?
11 of 20 similar drugs in Growth Hormone (GH) Deficiency were approved
Hype Score Breakdown
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01088412 | Pre-clinical | Completed |
Competing Products
20 competing products in Growth Hormone (GH) Deficiency
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Somatropin | Eli Lilly | Phase 3 | 40 |
| HER3-DXd | Daiichi Sankyo | Pre-clinical | 26 |
| Erlotinib | Astellas Pharma | Phase 2 | 27 |
| radio-labeled naquotinib + naquotinib | Astellas Pharma | Phase 1 | 21 |
| pegylated Somatropin + pegylated Somatropin + Jintropin AQ | Sun Pharmaceutical | Phase 2 | 35 |
| PEG-somatropin | Sun Pharmaceutical | Approved | 39 |
| PEG-somatropin + PEG-somatropin | Sun Pharmaceutical | Approved | 39 |
| PEG-somatropin | Sun Pharmaceutical | Phase 3 | 40 |
| Somatropin + Somatropin | Eli Lilly | Phase 3 | 40 |
| Somatropin + Somatropin | Eli Lilly | Phase 3 | 40 |
| somatropin, rDNA origin, for injection | Eli Lilly | Phase 3 | 40 |
| Sterile becaplermin gel vs. sterile placebo gel treatment 1 | Johnson & Johnson | Pre-clinical | 26 |
| ABT-414 | AbbVie | Pre-clinical | 26 |
| Saizen® A + Saizen® B | Merck | Phase 3 | 40 |
| Saizen® solution for injection (referred as Saizen®) | Merck | Approved | 43 |
| Cetuximab + FOLFIRI (5-Fluorouracil, Folinic acid, Irinotecan) | Merck | Phase 3 | 40 |
| Saizen + Saizen | Merck | Approved | 43 |
| Miransertib | Merck | Phase 2 | 39 |
| Miransertib | Merck | Phase 1/2 | 24 |
| ARX201 + ARX201 + ARX201 | Merck | Phase 2 | 35 |