Cumberland Pharmaceuticals

43 total trials 1 currently recruiting 37 completed

Cumberland Pharmaceuticals sponsors 43 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 37 completed. 23 of these trials are in Phase 3-4 (later-stage) and 19 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Hyponatremia, with 3 trials.

Trial Pipeline

43 total, page 1 of 1

RECRUITING Phase 2

Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF)

NCT05571059

ACTIVE NOT RECRUITING Phase 2

Oral Ifetroban to Treat Diffuse Cutaneous Systemic Sclerosis (SSc) or SSc-associated Pulmonary Arterial Hypertension

NCT02682511

COMPLETED Phase 2

Oral Ifetroban in Subjects With Duchenne Muscular Dystrophy

NCT03340675

COMPLETED Phase 2

Dose-ranging Efficacy and Pharmacokinetics Study of Intravenous Atorvastatin in Hypercholesterolemic Patients

NCT03611010

COMPLETED Phase 4

Safety and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients

NCT02583399

COMPLETED Phase 2

Oral Ifetroban to Treat Aspirin Exacerbated Respiratory Disease (AERD)

NCT03028350

COMPLETED Phase 2

Study to Assess Safety and Efficacy of Ifetroban for Treatment of Portal Hypertension in Cirrhotic Patients

NCT02802228

TERMINATED Phase 1

Telavancin Pediatric PK Study (Ages >12 Months to 17 Years)

NCT02013141

TERMINATED Phase 3

A Phase 3 Telavancin Staphylococcus Aureus (S. Aureus) Bacteremia Trial

NCT02208063

COMPLETED

Telavancin Observational Use Registry (TOUR)

NCT02288234

COMPLETED Phase 2

Trial to Determine the Safety of Oral Ifetroban in Patients With a History of Aspirin Exacerbated Respiratory Disease

NCT02216357

COMPLETED Phase 2

Efficacy and Safety of Bisacodyl and Lactulose as a Preparation for Colonoscopy

NCT02123017

COMPLETED Phase 2

2 Regimens of Lactulose for Colonoscopy Preparation in Adults

NCT01887470

COMPLETED Phase 4

Efficacy of Intravenous Ibuprofen Compared to Intravenous Ketorolac for Pain Control Following Arthroscopic Knee Surgery

NCT01901393

COMPLETED Phase 4

A Pilot Study to Determine the Efficacy of Intravenous Ibuprofen for Pain Control Following Arthroscopic Knee Surgery

NCT01650519

TERMINATED Phase 3

A Study to Assess the Efficacy, Safety and Pharmacokinetics of Intravenous Conivaptan (Vaprisol®) in Pediatric Subjects With Euvolemic or Hypervolemic Hyponatremia

NCT01451411

COMPLETED Phase 2

Safety and Pharmacokinetics of Ifetroban in Hepatorenal Syndrome Patients

NCT01436500

COMPLETED Phase 3

Safety and Efficacy of Intravenous Ibuprofen for Treatment of Pain in Pediatric Patients Undergoing Tonsillectomy

NCT01332253

COMPLETED Phase 4

Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen

NCT01334944

COMPLETED Phase 4

Surgical Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen

NCT01334957

COMPLETED Phase 1

A Study to Assess the Effect of Severe Hepatic Impairment on the Pharmacokinetics of Intravenous Conivaptan

NCT01370148

COMPLETED Phase 1

A Study to Evaluate the Effect of Renal Function on the Biological Activity of Telavancin

NCT01238796

TERMINATED Phase 3

Safety and Efficacy Study of a New Formulation of Acetylcysteine Injection

NCT01118663

COMPLETED Phase 3

Safety, Efficacy, and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients

NCT01002573

COMPLETED Phase 4

A Preference Study Comparing Kristalose® and Liquid Lactulose

NCT00712543

COMPLETED Phase 1

Study to Compare Conivaptan Pharmacokinetics in Subjects With Mild & Moderate Kidney Function Impairment to Subjects With Normal Kidney Function

NCT00887627

COMPLETED Phase 1

Study to Compare Conivaptan in Subjects With Mild & Moderate Liver Impairment Versus Subjects With Normal Liver Function

NCT00851227

COMPLETED Phase 3

Efficacy and Safety Study of Caldolor (Intravenous Ibuprofen) in Hospitalized Adult and Pediatric Burn Patients

NCT00606489

COMPLETED Phase 3

Efficacy and Safety Study of Caldolor (IV Ibuprofen) in Hospitalized Adult Orthopedic Patients

NCT00470600

COMPLETED Phase 3

Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia

NCT00478192

COMPLETED Phase 4

A Study of Multiple Dosing Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia

NCT00435591

COMPLETED Phase 3

A Study of Caldolor in Hospitalized Febrile Pediatric Patients

NCT00225706

COMPLETED Phase 3

Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus

NCT00107978

COMPLETED Phase 3

Comparison of Telavancin and Vancomycin for Hospital-acquired Pneumonia Due to Methicillin-resistant Staphylococcus Aureus

NCT00107952

COMPLETED Phase 3

Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus

NCT00091819

COMPLETED Phase 3

Trial of Caldolor for Treatment of Pain in Post-Operative Adult Patients

NCT00225732

COMPLETED Phase 3

An Open-Label Study of YM087 (Conivaptan) in Patients With Euvolemic or Hypervolemic Hyponatremia

NCT00379847

COMPLETED Phase 2

Phase 2 Trial of TD-6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)

NCT00077675

COMPLETED Phase 2

Telavancin for Treatment of Uncomplicated Staphylococcus Aureus Bacteremia

NCT00062647

COMPLETED Phase 2

Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)

NCT00061633

COMPLETED Phase 2

Safety and Efficacy Study of YM087 (Conivaptan) in Patients With Acute Decompensated Heart Failure

NCT00057356

COMPLETED Phase 3

Efficacy, Safety, and Pharmacokinetics of Intravenous Ibuprofen in Adult Febrile Patients

NCT01131000

COMPLETED Phase 3

Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia

NCT00380575

Phase Distribution

PhaseTrial count
Phase 1 5
Phase 2 14
Phase 3 16
Phase 4 7

What the Pipeline for Cumberland Pharmaceuticals Shows

According to the ClinicalTrials.gov registry, Cumberland Pharmaceuticals is linked to 43 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 2% of the sponsor's indexed portfolio, and 37 are already marked complete, representing roughly 86% of the total.

The phase mix for Cumberland Pharmaceuticals reports 23 late-stage studies (Phase 3 and Phase 4 combined) and 19 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Cumberland Pharmaceuticals is Hyponatremia with 3 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.