Sapientia Medicus Research

Our Studies

Indication Therapeutic Area   No. of Patients No. of Study
Gastroenterology Ulcerative Colitis 32 3
Crohn’s Disease 11 2
GERD 43 2
NAFLD 68 2
Oncology  Breast Cancer 12 1
Ovarian Cancer 9 1
Endocrinology  Diabetes Type II 98 4
Diabetes Type I 32 2
Thyroid   45 2
Rheumatology  Rheumatoid Arthritis 58 3
Ankylosing Spondylitis 49 2
SLE  17 2
Osteoarthritis  54 2
Pulmonology COPD 27 2
Asthma  35 2
Eosinophilic Asthma  17 1
Psychiatry Schizophrenia  28 2
Bipolar Disorder 26 1
Depression 48 2
Dermatology  Acne Vulgaris 21 3
Atopic Dermatitis 24 2
Psoriasis 28 2
Vaccine   COVID 19 1400 1
Cardiology Heart Failure   22 1
Neurology Multiple Sclerosis  13 1
Parkinson's Disease  12 1
Ophthalmology  Glaucoma  34 1
WET AMD 55 3
Flow Chart

Latest Achievements

CTRI/2024/08/072601

A Phase 2 Study to Evaluate MORF-057 in Adults with Moderately to Severely Active Crohn’s Disease

CTRI/2024/02/062456

A randomised, double blind, parallel, interventional phase IIa proof of concept trial to evaluate the efficacy and safety of ZYIL1 for the treatment of patients with mild to moderately active Ulcerative Colitis resistant or intolerant to oral amino salicylates 

CTRI/2023/09/057655

A Phase III, Randomized, Double blind, Parallel Group, Multicenter Study to Compare the Efficacy, Safety and Immunogenicity between Test Aflibercept and Eylea® in Patients with Neovascular (Wet) Age-Related Macular Degeneration (AMD) 

CTRI/2023/12/060909

A randomized, double-blind, placebo-controlled multicenter phase 3 study to evaluate efficacy, safety and tolerability of ianalumab on top of standard-of-care therapy in patients with systemic lupus erythematosus (SIRIUS-SLE 2) 

CTRI/2023/10/059345

A study to check out the effectiveness and safety of Lumateperone as another treatment used together with the main treatment in the Treatment of Patients with Major Depressive Disorder

CTRI/2023/05/053176

A randomized, double-blind, placebo-controlled, multicenter phase III study to evaluate the efficacy and safety of ABX464 once daily for induction treatment in subjects with moderately to severely active ulcerative colitis 

CTRI/2023/05/052628

A Multicenter, Randomized, Placebo and Active Comparator-Controlled Clinical Trial to Study the Efficacy, Safety and Pharmacokinetics (PK) of Tildrakizumab in Pediatric Subjects from 6 to less than 18 Years of Age with Moderate to Severe Chronic Plaque Psoriasis

CTRI/2023/02/050043

Phase 3 Multicenter, Randomized, Double-Blind, Study to Assess the Efficacy and Safety of Treatment with Bepirovirsen in HBeAg-negative Nucleos(t)ide Analogue-treated Participants with Chronic Hepatitis B Virus (B-Well 2) 

CTRI/2023/02/049923

Evaluate the effectiveness and safety of Elidel® in infants and children affected by mild to moderate Atopic dermatitis (AD) in India

CTRI/2022/11/047054

A phase 2 randomized, double-blind, parallel-group, placebo and active-controlled, two treatment period study to evaluate the safety and efficacy of Itolizumab for the induction of remission in biologics naïve patients with moderate to severely active ulcerative colitis

CTRI/2022/08/044563

A phase 3, multicenter, randomized, double-blind, double- dummy, parallel-group study to compare the efficacy and safety of fixed dose combination tablets of Dapagliflozin 10 mg and Linagliptin 5 mg versus Trajenta 5 mg(Linagliptin 5 mg) in patients with Type 2 Diabetes Mellitus(T2DM) inadequately controlled on Metformin 

CTRI/2020/11/029078

A Phase 4, open-label, single arm, 24-week, phase 4 study to evaluate the safety and efficacy of Mepolizumab 100 mg SC administered every 4 weeks in Indian participants aged ≥18 years with Severe eosinophilic asthma requiring oral corticosteroid treatment to Maintain asthma control (PRISM)