نتائج البحث

The Effect of Rectal Progesterone on the Latency period as well as Maternal and Prenatal Outcome in PPROM Between 24-33+6 Weeks قائمة الدراسات السريرية المسجلة على الادوية

Single arm Phase I/II study of the safety, tolerability and efficacy of the investigational anti PD-L1 monoclonal antibody Durvalumab in combination with Paclitaxel in patients with metastatic triple negative PD-L1 positive breast cancer قائمة الدراسات السريرية المسجلة على الادوية

An observational study to monitor the efficacy and tolerability of levofloxacin 250 mg OD for treatment of simple lower UTI in Saudi Arabia قائمة الدراسات السريرية المسجلة على الادوية

Diphtheria Toxoid/ Pertussis toxoid/ Tetanus Toxoid/ Filamentous haemagglutinin/ Inactivated Poliomyelitis virus type 1 (Mahoney strain)/ Inactivated Poliomyelitis virus type 2 (MEF-1 strain)/ Inactivated Poliomyelitis virus type 3 (Saukett strain) ,HAEMOPHILUS INFLUENZAE TYPE B Drug Safety Labeling

A Phase II/III, Extension Study of Orally Administered PHA-022121 for Acute Treatment of Angioedema Attacks in Patients with Hereditary Angioedema due to C1-Inhibitor Deficiency (Type I or Type II (RAPIDe-2) قائمة الدراسات السريرية المسجلة على الادوية

Diphtheria Toxoid/ Pertussis toxoid/ Tetanus Toxoid/ Filamentous haemagglutinin/ Inactivated Poliomyelitis virus type 1 (Mahoney strain)/ Inactivated Poliomyelitis virus type 2 (MEF-1 strain)/ Inactivated Poliomyelitis virus type 3 (Saukett strain) قائمة الأدوية تحت التسجيل / قائمة الأدوية المعروضة على لجنة التسجيل

سحب تشغيلتين من مستحضر (‎FELOCAINE (3% Prilocaine with Felypressin 0.03 IU/ML من إنتاج شركة RADIANT PARENTERAL LTD FOR ZYMETH - INDIA)) السحب و الإستدعاءات

A Phase III, Multicenter, Randomized, parallel-group study to asses the efficacy and saftey of double-blind pasireotide LAR 40 mg and pasireotide LAR 60 mg versus open lable octreotide LAR or lanreotide ATG in patients with inadequately controlled acromegaly. قائمة الدراسات السريرية المسجلة على الادوية

An Open-Label Study in Adolescent and Adult Severe (Coagulation Factor Activity <1%) Hemophilia A or B Patients With or Without Inhibitors Comparing Standard Treatment to PF-06741086 Prophylaxis قائمة الدراسات السريرية المسجلة على الادوية

An open label, Phase IV Multicentric Single Arm Study to Assess the Safety and Efficacy of BetazoleTM Cream Containing Betamethasone dipropionate (0.05% W/W) and Miconazole nitrate (2% W/W) in Subjects with Inflamed Skin Conditions of Eczema or Dermatitis 2ry Caused by Infection With Fungi قائمة الدراسات السريرية المسجلة على الادوية

عرض 1741 - 1750 من 1791