A Randomised, Phase II, Comparative Study With a Parallel Control for Evaluating the Efficacy and Safety of Combined Treatment of Lutropin Alpha and Recombinant Human Luteinizing Hormone in the Middle of the Controlled Ovarian Stimulation Follicular Phase in Women With Reduced Ovarian Reserve

NCT01110707 · clinicaltrials.gov ↗
PHASE2
Phase
COMPLETED
Status
131
Enrollment
INDUSTRY
Sponsor class

Conditions

Interventions

Sponsor

Merck KGaA, Darmstadt, Germany