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SUN PHARMACEUTICAL INDUSTRIES LIMITED

🇮🇳India
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

178

Active:35
Completed:73

Trial Phases

5 Phases

Phase 1:29
Phase 2:24
Phase 3:56
+2 more phases

Drug Approvals

120

PHILIPPINES:66
NMPA:20
FDA:11
+2 more agencies

Drug Approvals

Etoricoxib Tablets

Product Name
依托考昔片
Approval Number
国药准字HJ20230114
Approval Date
Oct 18, 2023
NMPA

Etoricoxib Tablets

Product Name
依托考昔片
Approval Number
国药准字HJ20230115
Approval Date
Oct 18, 2023
NMPA

Etoricoxib Tablets

Product Name
依托考昔片
Approval Number
国药准字HJ20230113
Approval Date
Oct 18, 2023
NMPA

Tildrakizumab Injection

Product Name
益路取
Approval Number
国药准字SJ20230006
Approval Date
May 26, 2023
NMPA

Tetrabenazine Tablets

Product Name
丁苯那嗪片
Approval Number
国药准字HJ20230050
Approval Date
May 12, 2023
NMPA

Tetrabenazine Tablets

Product Name
丁苯那嗪片
Approval Number
国药准字HJ20230051
Approval Date
May 12, 2023
NMPA

Rivastigmine Hydrogen Tartrate Capsules

Product Name
重酒石酸卡巴拉汀胶囊
Approval Number
国药准字HJ20181097
Approval Date
May 13, 2022
NMPA

Rivastigmine Hydrogen Tartrate Capsules

Product Name
重酒石酸卡巴拉汀胶囊
Approval Number
国药准字HJ20181098
Approval Date
May 13, 2022
NMPA

Paliperidone Extended-release Tablets

Product Name
帕利哌酮缓释片
Approval Number
国药准字HJ20220013
Approval Date
Mar 1, 2022
NMPA

Paliperidone Extended-release Tablets

Product Name
帕利哌酮缓释片
Approval Number
国药准字HJ20220014
Approval Date
Mar 1, 2022
NMPA
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Clinical Trials

Distribution across different clinical trial phases (159 trials with phase data)• Click on a phase to view related trials

Phase 3
56 (35.2%)
Phase 1
29 (18.2%)
Phase 4
26 (16.4%)
Phase 2
24 (15.1%)
Not Applicable
22 (13.8%)
phase_2_3
2 (1.3%)

A Study to Evaluate the Efficacy and Safety of Subcutaneous Tildrakizumab in Subjects With Moderate to Severe Genital Psoriasis.

Phase 3
Recruiting
Conditions
Moderate to Severe Genital Psoriasis
Interventions
First Posted Date
2024-09-24
Last Posted Date
2025-07-23
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
192
Registration Number
NCT06611163
Locations
🇺🇸

Medical Dermatology Specialists, Phoenix, Arizona, United States

🇺🇸

Smary Cures Clinical Research, Anaheim, California, United States

🇺🇸

California Dermatology & Clinical Research Institute, Encinitas, California, United States

and more 70 locations

A Study to Assess Sebaceous Gland Changes and Constituents of Sebum (Skin Oil) Induced by Clascoterone 1% Cream in Acne Patients

Phase 4
Active, not recruiting
Conditions
Acne Vulgaris
Interventions
First Posted Date
2024-05-23
Last Posted Date
2025-02-17
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
10
Registration Number
NCT06425900
Locations
🇺🇸

Dermatology Consulting Services, PLLC, High Point, North Carolina, United States

A Study to Evaluate the Impact of Clascoterone 1% Cream on Skin Barrier Properties in Acne Prone Patients

Phase 4
Completed
Conditions
Acne Vulgaris
Interventions
First Posted Date
2024-05-16
Last Posted Date
2025-03-04
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
50
Registration Number
NCT06415292
Locations
🇺🇸

Dermatology Consulting Services, PLLC, High Point, North Carolina, United States

A Study Evaluating the Efficacy and Safety of Clascoterone Cream 1% in Skin of Color Patients With Acne

Phase 4
Completed
Conditions
Acne Vulgaris
Interventions
First Posted Date
2024-05-16
Last Posted Date
2025-05-07
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
10
Registration Number
NCT06415305
Locations
🇺🇸

Skin Sciences, PLLC, Louisville, Kentucky, United States

A Study to Evaluate the Reduction in Sebum (Skin Oil) Induced by Clascoterone Cream 1% in Acne Patients

Phase 4
Completed
Conditions
Acne Vulgaris
Interventions
First Posted Date
2024-05-16
Last Posted Date
2025-04-15
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
40
Registration Number
NCT06415279
Locations
🇺🇸

Dermatology Consulting Services, PLLC, High Point, North Carolina, United States

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News

Sun Pharma's ILUMYA Achieves Primary Endpoints in Two Phase 3 Psoriatic Arthritis Trials

Sun Pharmaceutical Industries announced that tildrakizumab (ILUMYA) 100 mg successfully met primary endpoints in two Phase 3 clinical studies for active psoriatic arthritis treatment.

Sun Pharma Names Kirti Ganorkar as Managing Director in Major Leadership Transition

Kirti Ganorkar, a 29-year Sun Pharma veteran, will become Managing Director on September 1, 2025, succeeding founder Dilip Shanghvi who transitions to Executive Chairman.

Sun Pharma Discontinues Psoriasis and Eczema Drug SCD-044 After Phase 2 Trial Failures

Sun Pharma's experimental oral drug SCD-044 (Vibozilimod) failed to meet primary endpoints in Phase 2 trials for both psoriasis and atopic dermatitis, missing the 75% improvement target in PASI and EASI scores at 16 weeks.

FDA Approves Sun Pharma's Next-Generation LED BLU-U Device for Actinic Keratosis Treatment

The FDA has granted premarket approval for Sun Pharma's next-generation BLU-U Blue Light Photodynamic Therapy Illuminator, featuring LED panels instead of fluorescent tubes for treating actinic keratosis.

Sun Pharma Increases Investment in US-Based Pharmazz to Expand Specialty Therapeutics Portfolio

Sun Pharma has signed an agreement to invest up to $25 million in US-based Pharmazz, increasing its stake to approximately 22.7% on a fully diluted basis.

Sun Pharma and Moebius Medical's MM-II Shows Promising Results for Knee Osteoarthritis in Phase 2b Trial

A single injection of MM-II, a novel non-opioid treatment developed by Sun Pharma and Moebius Medical, demonstrated clinically meaningful pain relief for knee osteoarthritis lasting up to 26 weeks in a Phase 2b trial involving 397 patients.

Sun Pharma Launches Fexuclue in India: A Novel Treatment for Erosive Esophagitis

Sun Pharmaceutical has introduced Fexuclue (fexuprazan 40 mg), a novel potassium-competitive acid blocker, as a new treatment option for adults with all grades of erosive esophagitis in India.

Fortress Biotech Reports Strong 2024 Results with Two FDA Approvals and Strategic Acquisition Deal

Fortress Biotech secured FDA approvals for two key products in Q4 2024: Emrosi for inflammatory lesions of rosacea and UNLOXCYT for advanced cutaneous squamous cell carcinoma, with commercial launch of Emrosi already underway.

Lupin Launches First Generic Xarelto in US Market Despite Ongoing Patent Litigation

Lupin has begun rolling out the first generic version of the blockbuster anticoagulant Xarelto (rivaroxaban) in the US market after the Patent Trial and Appeal Board invalidated a key patent.

Sun Pharma to Acquire Checkpoint Therapeutics in $355 Million Deal for Novel Skin Cancer Treatment

Sun Pharmaceutical Industries will acquire Checkpoint Therapeutics for $355 million upfront, with stockholders receiving $4.10 per share plus a contingent value right worth up to $0.70 per share based on European approval milestones.

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