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Sun Pharmaceutical Industries clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, India and EU (CTIS) registers with Sun Pharmaceutical Industries as lead sponsor. Synced 26 Sep 2026
21Current trials
8Recruiting now
6Drugs in these trials
3Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Sun Pharmaceutical Industries is the lead sponsor of 21 current clinical trials in our USA, India and EU (CTIS) registers. 8 are recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are GL0034, Tildrakizumab and Abiraterone acetate. The most-studied condition is Type II Diabetes Mellitus.

ClinicalTrials.gov trials by status

  • Recruiting857%
  • Active, closed643%

Trials by phase

  • Phase 3643%
  • Phase 1214%
  • Phase 2/3214%
  • Phase 2214%
  • Observational17%
  • Phase 417%
01

Clinical trials sponsored by Sun Pharmaceutical Industries

14 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Safety Study for Prospective Assessment of Pregnancy Outcomes in Patients Treated With Tildrakizumab
NCT03992729 · Pregnancy Related
Observational Recruiting 2019-08 USA
Efficacy and Safety of GL0034 in Overweight or Obese Adults With Type II Diabetes Mellitus
NCT07282743 · ClinicalTrials.gov ↗ · Type II Diabetes Mellitus
Drug: GL0034
Phase 2 Recruiting 2026-01 USA, India
Study to Evaluate if Exposure to Drug is Impacted in Participants With Renal Insufficiency
NCT07385547 · Type II Diabetes Mellitus
Drug: GL0034
Phase 1 Recruiting 2026-02 USA
Study of Reformulated Levulan Kerastick Plus PDT for Actinic Keratosis on Upper Extremities
NCT07144852 · ClinicalTrials.gov ↗ · Actinic Keratosis
Phase 3 Recruiting 2025-11 USA
Study to Evaluate the Efficacy and Safety of Deuruxolitinib in Adolescents With Severe Alopecia Areata
NCT07133308 · ClinicalTrials.gov ↗ · Alopecia Areata
Phase 3 Recruiting 2025-08 USA
An Open-Label Pharmacokinetic Study for Patients With Actinic Keratosis on the Upper Extremities or the Face
NCT07729579 · ClinicalTrials.gov ↗ · Actinic Keratosis (AK)
Phase 1 Recruiting 2026-08 USA
Abiraterone, Enzalutamide, or Apalutamide in Castrate-sensitive Prostate Cancer.
NCT05422911 · ClinicalTrials.gov ↗ · Metastatic Cancer, Neoplasm, Prostate, Castrate-sensitive
Phase 2 Recruiting 2022-08 USA
Study of Reformulated Levulan Kerastick Plus PDT for Actinic Keratosis on Face and Scalp
NCT07144345 · ClinicalTrials.gov ↗ · Actinic Keratosis
Phase 3 Recruiting 2025-11 USA
A Study of Tildrakizumab in Pediatric Subjects With Chronic Plaque Psoriasis
NCT03997786 · ClinicalTrials.gov ↗ · Moderate-to-severe Chronic Plaque Psoriasis
Phase 2/3 Active, closed 2020-01 USA, India
Long Term Evaluation of Safety and Efficacy of Tildrakizumab in Patients With Psoriatic Arthritis
NCT04991116 · ClinicalTrials.gov ↗ · Psoriatic Arthritis
Phase 3 Active, closed 2022-06 USA, India
Efficacy and Safety of Tildrakizumab Compared to Placebo in Anti-TNF naïve Subjects With Active Psoriatic Arthritis II (INSPIRE 2)
NCT04314531 · ClinicalTrials.gov ↗ · Active Psoriatic Arthritis
Phase 3 Active, closed 2020-07 USA, India
A Study to Assess Sebaceous Gland Changes and Constituents of Sebum (Skin Oil) Induced by Clascoterone 1% Cream in Acne Patients
NCT06425900 · ClinicalTrials.gov ↗ · Acne Vulgaris
Phase 4 Active, closed 2024-07 USA
A Study to Evaluate the Efficacy and Safety of Subcutaneous Tildrakizumab in Subjects With Moderate to Severe Genital Psoriasis.
NCT06611163 · ClinicalTrials.gov ↗ · Moderate to Severe Genital Psoriasis
Phase 3 Active, closed 2025-03 USA
Extension Study to Evaluate Safety and Efficacy of CTP-543 in Adults With Alopecia Areata
NCT03898479 · ClinicalTrials.gov ↗ · Alopecia Areata
Phase 2/3 Active, closed 2019-04 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Sun Pharmaceutical Industries in the EU trials register (CTIS)

7 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with Sun Pharmaceutical Industries as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A first-in-human, randomized, double-blind, placebo-controlled, 3-part study assessing the safety, tolerability, pharmacodynamics and pharmacokinetics of GL0071 after single and repeated ascending subcutaneous doses in healthy normal weight, overweight and obese participants, as well as a 12-week treatment randomized, double blind, placebo-controlled exploratory Proof-of-Concept study in overweight and obese participants.
2025-524233-45-00 · Nutritional and Metabolic Diseases
Phase 1 Authorised Belgium
An open label, balanced, randomized, single dose, two-treatment, two period, two-sequence, crossover, bioequivalence study comparing Fexofenadine HCl and Pseudoephedrine HCl Extended Release Tablet 180 mg/240 mg, Manufactured by: Sun Pharmaceutical Industries Limited, India with Allegra-D® 24 HR (Fexofenadine HCl and Pseudoephedrine HCl Extended Release Tablets 180 mg + 240 mg) tablets, Distributed by: Chattem Inc., a Sanofi Company Chattanooga, TN 37409-0219, USA, in healthy, adult, human participants under fed conditions.
2026-525421-20-00 · CTIS ↗ · Immune System Diseases
Phase 1 Authorised Romania
An open label, balanced, randomized, single dose, two-treatment, four period, two-sequence, crossover, fully replicate, bioequivalence study comparing Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Extended Release Tablet USP 180 mg/240 mg, Manufactured by: Sun Pharmaceutical Industries Limited, India with Allegra-D® 24 HR (Fexofenadine HCl and Pseudoephedrine HCl Extended Release Tablets 180 mg + 240 mg) tablets, Distributed by: Chattem Inc., a Sanofi Company Chattanooga, TN 37409-0219, USA, in healthy, adult, human participants under fasting conditions.
2026-525420-22-00 · CTIS ↗ · Immune System Diseases
Phase 1 Authorised Romania
An open label, balanced, randomized, three treatment, three period, three sequence, single dose, crossover study to assess the effect of food and effect of apple sauce on bioavailability of the Test product (Bupropion Hydrochloride Extended Release Capsules 150 mg, manufactured by Sun Pharmaceutical Industries Limited, India) in healthy, adult, human subjects.
2025-523411-11-00 · CTIS ↗ · Mental Disorders
Phase 1 Authorised Romania
An open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose crossover, bioavailability study comparing Bupropion Hydrochloride Extended Release Capsules 150 mg, Manufactured by Sun Pharmaceutical Industries Limited, India with WELLBUTRIN XL (Bupropion hydrochloride) extended release tablets 300 mg, Distributed by: Bausch Health US, LLC Bridgewater, NJ 08807 USA. Manufactured by: Bausch Health Companies, Inc. Steinbach, MB R5G 1Z7, Canada, in healthy, adult, human subjects under fasting condition.
2025-523410-84-00 · CTIS ↗ · Mental Disorders
Phase 1 Authorised Romania
An open label, balanced, randomized, two-treatment, two-period, two-sequence, single-dose, crossover, bioequivalence study comparing Imatinib Mesylate Tablets 400 mg, manufactured by Sun Pharmaceutical Industries Limited, India with Glivec® (Imatinib mesylate) Coated tablets 400 mg, Produced by Novartis Pharma Produktions GmbH, Wehr, Germany or Novartis Pharmaceutical Manufacturing LLC, Ljubljana; Imported and Registered by Novartis Biosciences SA, Prof. Vicente Rao Avenue, 90, Sao Paulo – SP, CNPJ: 56.994.502/0001-30, Brazilian Industry, in healthy adult, human subjects under fed condition.
2025-524935-38-00 · CTIS ↗ · Neoplasms
Phase 1 Authorised Romania
An open label, balanced, randomized, two-treatment, two-period, two-sequence, single-dose, crossover bioequivalence study comparing Trametinib tablets 2 mg, Manufactured by Sun Pharmaceutical Industries Limited, India with MEKINIST® (Trametinib) tablets 2 mg, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, USA in healthy, adult, human subjects under fasting condition.
2025-524267-20-00 · CTIS ↗ · Neoplasms
Phase 1 Authorised Romania
03

Drugs in Sun Pharmaceutical Industries trials

6 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Sun Pharmaceutical Industries trials

14 conditions
Type II Diabetes Mellitus2Actinic Keratosis2Alopecia Areata2Pregnancy Related1Acne Vulgaris1Moderate-to-severe Chronic Plaque Psoriasis1Actinic Keratosis (AK)1Moderate to Severe Genital Psoriasis1Metastatic Cancer1Neoplasm, Prostate1Castrate-sensitive1Castrate-sensitive Prostate Cancer1Psoriatic Arthritis1Active Psoriatic Arthritis1
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA148
Clinical trials in India41
EU register (CTIS)7—

A trial with sites in more than one country appears in each of those registers.

06

Other sponsors in Type II Diabetes Mellitus

SponsorTrials
Corxel Pharmaceuticals1

Sponsors with the most current trials registered for this condition.

07

Questions about Sun Pharmaceutical Industries trials

How many clinical trials does Sun Pharmaceutical Industries sponsor?

Sun Pharmaceutical Industries is the lead sponsor of 14 current trials on ClinicalTrials.gov in our USA and India registers, and 7 authorised or ongoing trials in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Sun Pharmaceutical Industries trials recruiting?

Yes. 8 of its 14 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Sun Pharmaceutical Industries testing?

Its current trials name 6 drugs and biologicals as interventions. The most frequent are GL0034 (2), Tildrakizumab (2), Abiraterone acetate (1), Apalutamide (1) and Enzalutamide (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.