Nos essais cliniques

Efficacy and safety study of F373280 for maintenance of sinus rhythm after electrical cardioversion in patients with persistent Atrial Fibrillation and Chronic Heart Failure

Urodynamic effect of one single vaginal application of 2 mL of V0162 gel (0.8%) in post-menopausal women with overactive bladder

A 4-week double-blind placebo-controlled pilot study, evaluating niacin-induced flushing and lipid parameter effects of V0002 CA 1g 3 capsules/day associated with Niaspan® (from 375 mg to 1000 mg) in addition to usual care statin, in patients suffering from dyslipidemia with uncontrolled elevated triglycerides

Evaluation Of The Rate Of Pathological Complete Response (pCR) For Neoadjuvant Chemoradiotherapy (CT-RT) And For Chemotherapy (CT) Alone in Locally Advanced Non Small Cell Lung Cancer (LA-NSCLC): A Randomized Phase II trial

Efficacy and safety of 8% Clobetasol nail lacquer formulation versus vehicle in nail psoriasis

Essai clinique multicentrique, prospectif, en ouvert, contrôlé par appariement génotypique, pour étudier l'efficacité et la tolérance du traitement prénatal par ER004 administré par voie intra-amniotique chez des sujets de sexe masculin atteints de dysplasie ectodermique hypohidrotique liée à l'X (XLHED).

V0251 oral suspension efficacy and tolerance in vestibular neuritis. A randomised double-blind placebo controlled study

Étude de phase II multicentrique en ouvert avec phase de test de la tolérance (safety lead-in) évaluant l’efficacité, la tolérance et la pharmacocinétique de l’association encorafénib et binimétinib chez des participants chinois atteints d’un cancer du poumon métastatique non à petites cellules avec mutation BRAF^V600E n’ayant pas reçu de traitement préalable par inhibiteurs de BRAF et de MEK.

A dose-finding study of efficacy and safety of F13640 in patients with moderate to severe painful peripheral diabetic polyneuropathy

Efficacy and tolerance of V0071 GM 01A in inflammatory seborrhoeic dermatitis of the scalp.

Proof of Concept study of the efficacy and tolerability of a 4-week treatment with F13640 in patients in whom the adaptation of opioid therapy of cancer pain has failed. A prospective, multinational, multicentre, randomised, double-blind, placebo-controlled study.

Prospective randomised phase II trial of oral vinorelbine and cisplatin or pemetrexed and cisplatin in first line Metastatic or Locally Advanced Non-Small-Cell Lung Cancer patients with non-squamous histological type

A double blind, multinational, multicentre, placebo controlled 10-week study assessing the efficacy and safety of F2695 SR flexible dose (75, 100 mg/day) in the treatment of patients with major depression

Phase II study evaluating oral vinorelbine as a single agent in patients with hormone receptor breast cancer with bone metastases previously treated by a hormone therapy

Efficacy of the topic RV3131A-HC3221 in the prevention of polymorphic light eruption

Randomised, double-blind, placebo-controlled dose-effect study of V0114 (2.5, 5, 7.5 and 10 mg) versus mequitazine 10 mg and placebo in the treatment of seasonal allergic rhinitis

Randomised Phase II Study comparing, as first-line chemotherapy, single-agent Oral Vinorelbine administered with two different schedules in patients with Advanced Breast Cancer

Un essai de phase 2 multicentrique randomisé en ouvert, avec phase de test de la tolérance (safety lead-in), évaluant l’association encorafénib et cétuximab versus irinotécan/cétuximab ou 5-fluorouracil (5-FU) /acide folinique (AF)/irinotécan (FOLFIRI)/cétuximab chez des participants chinois atteints de cancer colorectal métastatique avec mutation BRAFV600E.

Efficacy study of Ciclopiroxolamine 1% foam (DC115 GM 02A) versus Ciclopiroxolamine 1.5% shampoo (SEBIPROX®) in the treatment of moderate seborrheic dermatitis of the scalp

Phase II study assessing the maintenance treatment with vinflunine after first-line therapy with gemcitabine and cisplatin in patients with advanced or metastatic transitional cell carcinoma of the urothelial tract