Luveris (lutropin alfa)
- Region
- 🇪🇺 EU
- Active substance
- lutropin alfa
- Company
- Merck Europe B.V.
- Status
- Authorised
- Therapeutic area
- Ovulation Induction; Infertility, Female
- EU approval
- Wed 29 Nov 2000
- Application
- EMEA/H/C/000292
- ATC
- G03GA07
- Official record
- www.ema.europa.eu
Indication
Luveris in association with a follicle-stimulating-hormone (FSH) preparation is recommended for the stimulation of follicular development in women with severe luteinising-hormone (LH) and FSH deficiency. In clinical trials, these patients were defined by an endogenous serum LH level <1.2 IU/l.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Pergoveris Authorised · Merck Europe B.V.
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.