Cumberland Pharmaceuticals
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
Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF)
NCT05571059
Oral Ifetroban to Treat Diffuse Cutaneous Systemic Sclerosis (SSc) or SSc-associated Pulmonary Arterial Hypertension
NCT02682511
Oral Ifetroban in Subjects With Duchenne Muscular Dystrophy
NCT03340675
Dose-ranging Efficacy and Pharmacokinetics Study of Intravenous Atorvastatin in Hypercholesterolemic Patients
NCT03611010
Safety and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients
NCT02583399
Oral Ifetroban to Treat Aspirin Exacerbated Respiratory Disease (AERD)
NCT03028350
Study to Assess Safety and Efficacy of Ifetroban for Treatment of Portal Hypertension in Cirrhotic Patients
NCT02802228
Telavancin Pediatric PK Study (Ages >12 Months to 17 Years)
NCT02013141
A Phase 3 Telavancin Staphylococcus Aureus (S. Aureus) Bacteremia Trial
NCT02208063
Telavancin Observational Use Registry (TOUR)
NCT02288234
Trial to Determine the Safety of Oral Ifetroban in Patients With a History of Aspirin Exacerbated Respiratory Disease
NCT02216357
Efficacy and Safety of Bisacodyl and Lactulose as a Preparation for Colonoscopy
NCT02123017
2 Regimens of Lactulose for Colonoscopy Preparation in Adults
NCT01887470
Efficacy of Intravenous Ibuprofen Compared to Intravenous Ketorolac for Pain Control Following Arthroscopic Knee Surgery
NCT01901393
A Pilot Study to Determine the Efficacy of Intravenous Ibuprofen for Pain Control Following Arthroscopic Knee Surgery
NCT01650519
A Study to Assess the Efficacy, Safety and Pharmacokinetics of Intravenous Conivaptan (Vaprisol®) in Pediatric Subjects With Euvolemic or Hypervolemic Hyponatremia
NCT01451411
Safety and Pharmacokinetics of Ifetroban in Hepatorenal Syndrome Patients
NCT01436500
Safety and Efficacy of Intravenous Ibuprofen for Treatment of Pain in Pediatric Patients Undergoing Tonsillectomy
NCT01332253
Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen
NCT01334944
Surgical Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen
NCT01334957
A Study to Assess the Effect of Severe Hepatic Impairment on the Pharmacokinetics of Intravenous Conivaptan
NCT01370148
A Study to Evaluate the Effect of Renal Function on the Biological Activity of Telavancin
NCT01238796
Safety and Efficacy Study of a New Formulation of Acetylcysteine Injection
NCT01118663
Safety, Efficacy, and Pharmacokinetic Study of Intravenous Ibuprofen in Pediatric Patients
NCT01002573
A Preference Study Comparing Kristalose® and Liquid Lactulose
NCT00712543
Study to Compare Conivaptan Pharmacokinetics in Subjects With Mild & Moderate Kidney Function Impairment to Subjects With Normal Kidney Function
NCT00887627
Study to Compare Conivaptan in Subjects With Mild & Moderate Liver Impairment Versus Subjects With Normal Liver Function
NCT00851227
Efficacy and Safety Study of Caldolor (Intravenous Ibuprofen) in Hospitalized Adult and Pediatric Burn Patients
NCT00606489
Efficacy and Safety Study of Caldolor (IV Ibuprofen) in Hospitalized Adult Orthopedic Patients
NCT00470600
Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia
NCT00478192
A Study of Multiple Dosing Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia
NCT00435591
A Study of Caldolor in Hospitalized Febrile Pediatric Patients
NCT00225706
Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus
NCT00107978
Comparison of Telavancin and Vancomycin for Hospital-acquired Pneumonia Due to Methicillin-resistant Staphylococcus Aureus
NCT00107952
Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus
NCT00091819
Trial of Caldolor for Treatment of Pain in Post-Operative Adult Patients
NCT00225732
An Open-Label Study of YM087 (Conivaptan) in Patients With Euvolemic or Hypervolemic Hyponatremia
NCT00379847
Phase 2 Trial of TD-6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
NCT00077675
Telavancin for Treatment of Uncomplicated Staphylococcus Aureus Bacteremia
NCT00062647
Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
NCT00061633
Safety and Efficacy Study of YM087 (Conivaptan) in Patients With Acute Decompensated Heart Failure
NCT00057356
Efficacy, Safety, and Pharmacokinetics of Intravenous Ibuprofen in Adult Febrile Patients
NCT01131000
Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia
NCT00380575
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 5 |
| Phase 2 | 14 |
| Phase 3 | 16 |
| Phase 4 | 7 |
Therapeutic Areas
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.