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| Study Title | Study Sponsor | Status | Study Drug | Trial Phase | Study Protocol Number | Site |
|---|---|---|---|---|---|---|
| A Multicenter, Multinational, Extension Study to Evaluate the Long-Term Efficacy and Safety of BMN 110 in Patients With Mucopolysaccharidosis IVA (Morquio A Syndrome) | BioMarin Pharmaceutical Inc. | Completed | BMN 110 | 3 | MOR-005 | KFSH & RC-R |
| A Double-Blind, Randomized, Placebo-Controlled, Phase 3 Study to Demonstrate Efficacy and Safety of A4250 in Children with Progressive Familial Intrahepatic Cholestasis Types 1 and 2 (PEDFIC 1) | Albireo | Completed | A4250-005 | 3 | A4250-005 | KFSH&RC-R |
| A Double-Blind Randomized Phase III Study Evaluating the Efficacy and Safety of Sorafenib Compared to Placebo in Locally Advanced/Metastatic RAI-Refractory Differentiated Thyroid Cancer | Bayer | Completed | Sorafenib | 3 | BAY43-9006/14295 | KFSH & RC-R |
| A Compartive Multicenter Study of Neoadjuvant Docetaxel/Cisplatin Followed by Concurrent Cisplatin with Radiotherapy using Intensity-Modulated Radition Therapy (IMRT) with or without Bevacizumab for Locally Advanced Nasopharyngeal Cancer | King Fahad Medical City | Completed | Docetaxel/Cisplatin and Bevacizumab | 3 | Version 1.3 date 6 may 2012 | KFMC |
| A 96-week, two-arm, randomized, single-masked, multicenter, phase III study assessing the efficacy and safety of brolucizumab 6 mg compared to panretinal photocoagulation laser in patients with proliferative diabetic retinopathy (CONDOR) | Novartis | Completed | Brolucizumab | 3 | CRTH258D2301 | DESH |
| A 52-Week, Open-Label, Prospective, Multicenter, International Study of a Transition to the Paliperidone Palmitate 3-Month Formulation in Patients with Schizophrenia Previously Stabilized on the Paliperidone Palmitate 1-Month Formulation | anssen-Cilag International NV | Completed | paliperidone | 3 | R092670SCH3015 | JPH |
| A 52-week, double-blind, randomised, multi-centre, phase III, parallel-group study in patients 12 years and older with asthma, evaluating the efficacy and safety of Symbicort (budesonide/formoterol) Turbuhaler 160/4.5 μg 'as needed' compared with Pulmicort (budesonide) Turbuhaler 200 μg twice daily plus terbutaline Turbuhaler 0.4 mg 'as needed' | AstraZeneca | Completed | Budesonide + Formoterol VS. Budesonide + Terbutaline | 3 | D589SC00003 | AFH-DH |
| A 3 Month, Multicenter, Double-Masked Safety and Efficacy Study of Travoprost Ophthalmic Solution, 0.004% Compared to Timolol (0.5% or 0.25%) in Pediatric Glaucoma Patients | Alcon | Completed | Travoprost 0.004% / Timolol | 3 | C-12-008 | KKESH |
| A 2-treatment period, randomized, placebo-controlled, multicenter parallel-group study to assess the safety of QAW039 when added to existing asthma therapy in GINA steps 3, 4 and 5 patients with uncontrolled asthma | Novartis | Terminated | QAW039/Fevipiprant | 3 | CQAW039A2315 | KFMC |
| A 2-treatment period, randomized, placebo-controlled, multicenter parallel-group study to assess the safety of QAW039 when added to existing asthma therapy in GINA steps 3, 4 and 5 patients with uncontrolled asthma | Novartis | Terminated | QAW039/Fevipiprant | 3 | CQAW039A2315 | KFMC |
Last update date: 08/05/2025 at 03:17 PM Saudi Arabia time
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