Roxane Laboratories

93 total trials 92 completed

Roxane Laboratories sponsors 93 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 92 completed. 2 of these trials are in Phase 3-4 (later-stage) and 16 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Breast Cancer, with 4 trials.

Trial Pipeline

93 total, page 2 of 2

COMPLETED NA

Bioequivalency Study of Levetiracetam 750 mg Tablets Under Fed Conditions

NCT00826787

COMPLETED NA

A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Balsalazide Disodium 750 mg Capsules Under Fasting Conditions

NCT00618202

COMPLETED NA

Bioequivalency Study of Meloxicam Tablets Under Fasting Conditions

NCT00618163

COMPLETED NA

Bioequivalency Study of Meloxicam Tablets Under Fed Conditions

NCT00601887

COMPLETED NA

A Single Dose, 4-Period, 2-Treatment Replicate Design Bioequivalency Study of Granisetron Hydrochloride 1 mg Tablets Under Fasting Conditions

NCT00618254

COMPLETED NA

A Single Dose, 4-Period, 2-Treatment Replicate Design Bioequivalency Study of Granisetron Hydrochloride 1 mg Tablets Under Fed Conditions

NCT00618111

COMPLETED NA

Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide 100 mg /25 mg Tablet Under Fed Conditions

NCT01102465

COMPLETED NA

Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide 100 mg/25 mg Tablet Under Fasted Conditions

NCT01102478

COMPLETED NA

Bioequivalency Study of Ramipril 10 mg Capsules Under Fed Conditions

NCT00702260

COMPLETED NA

Bioequivalency Study of Ramipril 10 mg Capsules Under Fasting Conditions

NCT00702091

COMPLETED NA

Bioequivalency Study of Oxcarbazepine 600 mg Tablets Under Fed Conditions

NCT00618046

COMPLETED NA

Bioequivalency Study of Exemestane 25 mg Tablet Under Fed Conditions

NCT01331434

COMPLETED NA

Bioequivalency Study of Losartan Potassium 100 mg Tablet Under Fed Conditions

NCT01216878

COMPLETED NA

Bioequivalency Study of 7.5 mg Pilocarpine Tablets Under Fasting Conditions

NCT00602524

COMPLETED NA

Bioequivalency Study of 7.5 mg Pilocarpine Under Fed Conditions

NCT00618059

COMPLETED NA

Bioequivalency Study of Losartan Potassium 100 mg Tablet Under Fasted Conditions

NCT01216852

COMPLETED NA

Bioequivalency Study of Exemestane 25 mg Tablet Under Fasted Conditions

NCT01331421

COMPLETED NA

Pilot Bioequivalency Study of Exemestane 25 mg Tablet Under Fasted Conditions

NCT01331447

COMPLETED NA

Bioequivalency Study of Amlodipine Tablets Under Fasting Conditions

NCT00602017

COMPLETED NA

Bioequivalency Study of Amlodipine Tablets Under Fed Conditions

NCT00601302

COMPLETED NA

Bioequivalency Study of Terbinafine Tablets Under Fed Conditions

NCT00602251

COMPLETED NA

Bioequivalency Study of Zolpidem Tartrate Under Fed Conditions

NCT00602719

COMPLETED NA

Bioequivalency Study of Terbinafine Tablets Under Fasting Conditions

NCT00602342

COMPLETED NA

Bioequivalency Study of Zolpidem Tartrate Under Fasting Conditions

NCT00601666

COMPLETED NA

Bioequivalency Study of Zaleplon 10 mg Capsules Under Fed Conditions

NCT00694317

COMPLETED NA

Bioequivalency Study of 50 mg Cilostazol Tablets Under Fasting Conditions

NCT00602407

COMPLETED NA

Bioequivalency Study of Zaleplon 10 mg Capsules Under Fasting Conditions

NCT00694187

COMPLETED NA

Bioequivalency Study of Balsalazide Capsules Under Fasting Conditions

NCT00618228

COMPLETED NA

Bioequivalency Study of 5 mg Piolocarpine Tablets Under Fed Conditions

NCT00601211

COMPLETED NA

Bioequivalency Study of Torsemide Tablets Under Fasting Conditions

NCT00602303

COMPLETED NA

Bioequivalency Study of Torsemide Tablets Under Fed Conditions

NCT00602615

COMPLETED NA

Bioequivalency Study of 5 mg Pilocarpine Tablets Under Fasting Conditions

NCT00601874

COMPLETED NA

Bioequivalency Study of Calcitriol Tablets Under Fasting Conditions

NCT00601328

COMPLETED NA

Bioequivalency Study of Zidovudine Under Fasting Conditions

NCT00602550

COMPLETED NA

Bioequivalency Study of Zidovudine Under Fed Conditions

NCT00601562

COMPLETED NA

Bioequivalency Study of 300 mg Lithium Carbonate Under Fed Conditions

NCT00602394

COMPLETED NA

Bioequivalency Study of 100 mg Cilostazol Tablets Under Fasting Conditions

NCT00602173

COMPLETED NA

Bioequivalency Study of Clarithromycin Tablets Under Fasting Conditions

NCT00601315

COMPLETED NA

Bioequivalency Study of 300 mg Lithium Carbonate Under Fasting Conditions

NCT00601536

COMPLETED NA

Bioequivalency Study of Clarithromycin Tablets Under Fed Conditions

NCT00602498

COMPLETED NA

Bioequivalency Study of 450 mg Lithium Carbonate Under Fasting Conditions

NCT00602381

COMPLETED NA

Bioequivalence Study of 6-Mercaptopurine Under Fasting Conditions

NCT00602134

COMPLETED NA

Bioequivalency Study of 450 mg Lithium Carbonate Under Fed Conditions

NCT00601575

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Phase Distribution

PhaseTrial count
Phase 1 16
Phase 3 1
Phase 4 1

What the Pipeline for Roxane Laboratories Shows

According to the ClinicalTrials.gov registry, Roxane Laboratories is linked to 93 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 92 are already marked complete, representing roughly 99% of the total.

The phase mix for Roxane Laboratories reports 2 late-stage studies (Phase 3 and Phase 4 combined) and 16 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Roxane Laboratories is Breast Cancer with 4 linked trials, and 9 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.