Dr. Reddy's Laboratories Limited

52 total trials 51 completed

Dr. Reddy's Laboratories Limited sponsors 52 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 51 completed. 10 of these trials are in Phase 3-4 (later-stage) and 42 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Healthy, with 6 trials.

Trial Pipeline

52 total, page 1 of 2

COMPLETED Phase 3

A Phase III Transition Study of DRL Rituximab to Reference Medicinal Products

NCT04268771

COMPLETED Phase 3

Compare Efficacy, Safety, and Immunogenicity of Proposed Rituximab Biosimilar (DRL_RI) With MabThera® in LTB Follicular Lymphoma

NCT03976102

COMPLETED Phase 2

Efficacy, Tolerability, Safety, and Pharmacokinetic Study of DFN-15

NCT03554772

COMPLETED Phase 2

A Study to Assess the Efficacy and Safety of PPC-06 (Tepilamide Fumarate)

NCT03421197

COMPLETED Phase 2

A Bioavailability Study of DFD-03 Compared to Tazorac® in Patients With Moderate Acne Vulgaris

NCT03599193

COMPLETED Phase 2

A Study to Assess the Safety and Local Tolerability of DFD-03 (Tazarotene) Lotion, 0.1% Compared to Tazorac® Cream, 0.1% in the Topical Treatment of Acne Vulgaris

NCT03341910

COMPLETED Phase 3

A Study of the Safety and Efficacy of DFD-03 for the Treatment of Acne Vulgaris

NCT03290027

COMPLETED Phase 3

A Study of the Safety and Efficacy of DFD-03 Lotion in the Treatment of Acne Vulgaris for 12 Weeks

NCT03292640

COMPLETED Phase 1

Study on the Pharmacokinetics (PK) of DFN-15 vs Comparator and Food-effect on DFN-15 PK in Healthy Adult Subjects

NCT03282838

COMPLETED Phase 2

A Study to Evaluate Two Concentrations of DFD-07 Cream, in Subjects With Actinic Keratosis (AK) of the Face and/or Scalp Over a 12-week Treatment Period

NCT03116698

COMPLETED Phase 3

DFN-11 Injection in Episodic Migraine With or Without Aura

NCT02569853

COMPLETED Phase 2

Pilot Study of Two Different Strengths of DFN-11 Injection for Rapidly Escalating Migraine

NCT02571049

COMPLETED Phase 3

A Study to Evaluate the Therapeutic Equivalence of Generic Permethrin Cream 5% to Elimite® in the Treatment of Scabies

NCT02572986

TERMINATED Phase 2

Pilot Study of DFN-11 Injection in Medication Overuse Headache

NCT02583425

COMPLETED Phase 1

Bioavailability of DFN-15 at 3 Different Doses vs. Comparator and to Determine Dose-proportionality of DFN-15 in Fasting Healthy Adults

NCT03051685

COMPLETED Phase 2

Two Dose Levels of DFN-15 vs. Placebo in Patients With Migraine Headaches

NCT02472418

COMPLETED Phase 3

DFN-02 Open Label Safety Study in Patients With Acute Migraine

NCT02279082

COMPLETED Phase 2

A Study to Assess the Efficacy and Safety of XP23829 in Subjects With Moderate-to-Severe Chronic Plaque-Type Psoriasis

NCT02173301

COMPLETED Phase 3

A Study of the Efficacy and Safety of Abametapir Lotion Administered for the Treatment of Head Lice Infestation

NCT02060903

COMPLETED Phase 3

Study of the Efficacy and Safety of Abametapir Lotion Administered for the Treatment of Head Lice Infestation

NCT02062060

COMPLETED Phase 1

Dermal Safety Study to Evaluate Potential Irritation of Abametapir Lotion

NCT02061813

COMPLETED Phase 1

Dermal Safety Study to Evaluate the Sensitizing Potential of Abametapir Lotion

NCT02062073

COMPLETED Phase 2

Safety, Efficacy and Tolerability Study of up to 20 mL of DFA-02 in Patients Undergoing Abdominal Surgery

NCT01888367

COMPLETED Phase 2

A Pediatric Safety and Pharmacokinetics Study of Ha44 Gel Administered Topically for Treatment of Head Lice Infestation

NCT02010333

COMPLETED Phase 3

Evaluation of Clinical Equivalence Between Two Lubiprostone Products in the Treatment of Chronic Idiopathic Constipation

NCT01674530

COMPLETED Phase 1

DFA-02 in Patients Undergoing Colorectal Surgery

NCT01496352

COMPLETED Phase 1

Study to Evaluate the Effect of Ha44 Gel on the Electrocardiogram in Healthy Volunteers

NCT01518699

COMPLETED Phase 2

An Efficacy and Safety Study of Ha44 Gel Administered Topically for the Treatment of Head Lice Infestation

NCT01336647

COMPLETED Phase 1

Bioequivalence Study of Finasteride 5 mg Tablet Formulations Under Fasting Conditions

NCT01264289

COMPLETED Phase 1

Bioequivalence Study of Two Finasteride 5 mg Tablet Formulations Under Non-Fasting Conditions

NCT01264302

COMPLETED Phase 1

Bioequivalence Study of Desloratadine and Pseudoephedrine Extended-release Tablets Under Fed Conditions

NCT01506791

COMPLETED Phase 1

Bioequivalence Study for Desloratadine OD Tablets 5 mg Under Fed Condition

NCT01506037

COMPLETED Phase 1

Bioequivalence Study for Desloratadine OD Tablets 5 mg Under Fasting Condition

NCT01506050

COMPLETED Phase 1

Bioavailability Study of Desloratadine 5 mg Tablet of Dr. Reddy's Under Fed Conditions

NCT01314352

COMPLETED Phase 1

Bioavailability Study of Dr. Reddy's Desloratadine Tablets, 5 mg Under Fasting Conditions.

NCT01314339

COMPLETED Phase 1

Bioavailability Study of Ciprofloxacin 1000 mg ER Tablets of Dr. Reddy's Under Fasting Conditions

NCT01372345

COMPLETED Phase 1

Bioequivalence Study of Zonisamide Capsules 100 mg of Dr.Reddy's Laboratories Limited Under Fed Conditions

NCT01161979

COMPLETED Phase 1

Bioequivalence Study of Zonisamide Capsules 100 mg of Dr.Reddy's Laboratories Limited Under Fasting Conditions

NCT01161966

COMPLETED Phase 1

Bioavailability Study of Ciprofloxacin 1000 mg ER Tablets of Dr. Reddy's Under Non-Fasting Conditions

NCT01372358

COMPLETED Phase 1

Bioequivalence Study of Ziprasidone HCL Capsules, 20 mg of Dr. Reddy's Under Fed Conditions

NCT01581879

COMPLETED Phase 1

Bioequivalence Study of Ziprasidone HCL Capsules, 20 mg Under Fasting Conditions

NCT01581866

COMPLETED Phase 1

Bioavailability Study of Levetiracetam Tablets, 750 mg of Dr. Reddy's Under Fasting Conditions.

NCT01131897

COMPLETED Phase 1

Bioequivalence Study of Levetiracetam Tablets, 750 mg of Dr. Reddy's Under Fed Conditions

NCT01132352

COMPLETED Phase 1

Bioequivalence Study of Lamotrigine 25 mg Chewable Tablets of Dr.Reddy's Under Fed Condition

NCT01131975

COMPLETED Phase 1

Bioequivalence Study of Lamotrigine 25 mg Chewable Tablets of Dr.Reddy's Under Fasting Condition

NCT01131949

COMPLETED Phase 1

Bioequivalence Study for Lamotrigine Tablets 200 mg Under Fasting Condition

NCT01513720

COMPLETED Phase 1

Bioequivalence Study for Lamotrigine Tablets 200 mg Under Fed Condition

NCT01513681

COMPLETED Phase 1

Bioequivalency Study of Amlodipine Besylate Tablets, 10 mg of Dr. Reddy's Under Fasting Conditions

NCT01131923

COMPLETED Phase 1

Bioequivalence Study of Isotretinoin Capsules 20 mg Under Fasting Condition

NCT01888341

COMPLETED Phase 1

Bioequivalency Study of Amlodipine Besylate Tablets, 10 mg of Dr. Reddy's Under Fed Conditions

NCT01131936

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Phase Distribution

PhaseTrial count
Phase 1 30
Phase 2 12
Phase 3 10

What the Pipeline for Dr. Reddy's Laboratories Limited Shows

According to the ClinicalTrials.gov registry, Dr. Reddy's Laboratories Limited is linked to 52 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 51 are already marked complete, representing roughly 98% of the total.

The phase mix for Dr. Reddy's Laboratories Limited reports 10 late-stage studies (Phase 3 and Phase 4 combined) and 42 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Dr. Reddy's Laboratories Limited is Healthy with 6 linked trials, and 8 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.