Prospective multicentre non-interventional study to assess the patterns of use of rekovelle in women undergoing in vitro fertilisation or intracytoplasmic sperm injection procedures in routine clinical practice
LIBERTY 2: An international phase 3 randomized, double-blind, placebo-controlled efficacy and safety study to evaluate relugolix co administered with and without low-dose estradiol and norethindrone acetate in women with heavy menstrual bleeding associated with uterine fibroids
An international phase 3 randomized, double-blind, placebo-controlled efficacy and safety study to evaluate relugolix administered with and without low-dose estradiol and norethindrone acetate in women with endometriosis-associated pain
A phase 3, randomized, parallel-group, multicenter, open-label, pharmacokinetic, noninferiority study of ravulizumab administered subcutaneously versus intravenously in adult patients with paroxysmal nocturnal hemoglobinuria currently treated with eculizumab
Randomized phase 3 study evaluating the efficacy and the safety of oral azacitidine (CC-486) compared to investigator’s choice therapy in patient with relapsed or refractory angioimmunoblastic T- cell lymphoma
A phase II study of brentuximab vedotin in patients with relapsed or refractory peripheral T-cell lymphoma treated with gemcitabine followed by brentuximab vedotin maintenance
Effects of plasma exchange with human serum albumin 5% (PE-A 5%) on short-term survival in subjects with “acute-on-chronic liver failure” (ACLF) at high risk of hospital mortality
A phase 1b open-label study assessing the pharmacokinetics, tolerability, and safety of oral trimetazidine in subjects with acute-on-chronic liver failure - trust: trimetazidine for acute on chronic liver failure study
Prodige 34-etude de phase 3 randomisée évaluant la chimiothérapie adjuvante après résection d’un adénocarcinome colique de stade 3 chez les patients de 70 ans et plus (adage)
A phase 4, double-blind, randomized, placebo-controlled study evaluating the pharmacokinetics and safety of obeticholic acid in patients with primary biliary cholangitis and moderate to severe hepatic impairment