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Eagle Pharmaceuticals, Inc. Clinical Trials

Eagle Pharmaceuticals, Inc. Clinical Trials

Studies registered on ClinicalTrials.gov (U.S. National Library of Medicine) with the company as lead sponsor or collaborator, newest start first. Values are as registered.

  • 2026-09-15: Study NCT07325227; Company role Collaborator; Phase Phase 4; Status Not yet recruiting.
  • 2023-07-22: Study NCT05776004; Company role Lead sponsor; Phase Phase 2; Status Active not recruiting.
  • 2018-08-19: Study NCT03600376; Company role Lead sponsor; Phase Phase 3; Status Completed.
  • 2017-11-30: Study NCT03324061; Company role Lead sponsor; Phase Phase 1; Status Completed.
Start dateStudyCompany rolePhaseStatusConditionsEnrollmentCompletion date
2026-09-15NCT07325227
Study of Remimazolam for Cataract Surgery
Collaborator
Lead: Fred E, Shapiro
Phase 4Not yet recruitingCataract Surgery Anesthesia302028-06-01
2023-07-22NCT05776004
Blinded Efficacy and Safety Study of CAL02 IV Plus SOC in Subjects With Severe Community-Acquired Bacterial Pneumonia
Lead sponsorPhase 2Active not recruitingPneumonia, Bacterial2762026-09-07
2018-08-19NCT03600376
Study to Assess the Efficacy and Safety of Ryanodex as Adjuvant Treatment in Subjects With EHS
Lead sponsorPhase 3Completed
Results posted
Exertional Heat Stroke172019-08-14
2017-11-30NCT03324061
Study to Evaluate the Safety, Tolerability, and PK of Fulvestrant After IM Administration
Lead sponsorPhase 1CompletedPharmacokinetics6002018-07-12
2017-08-12NCT03189433
Efficacy and Safety Study of Ryanodex as Adjuvant Treatment in Subjects With Psychostimulant Drug-Induced Toxicity (PDIT)
Lead sponsorPhase 2Terminated
Results posted
Drug Toxicity Psychotropic Agents Psychostimulants22018-12-31
2015-09NCT02513095
Efficacy and Safety of Ryanodex® (EGL-4104) as Adjuvant Treatment in Subjects With Exertional Heat Stroke (EHS)
Lead sponsorPhase 2Completed
Results posted
Heat Stroke342015-10
2013-11NCT02162888
A Phase I, Bioequivalence Study to Evaluate Two Formulations of Bendamustine (BDM) Hydrochloride (HCl) Administered to Cancer Patients
Lead sponsorPhase 1CompletedCancer Which Has Either Progressed or Relapsed After Standard Therapy, or for Which no Curative or Standard Therapy is Appropriate812014-11
2008-01NCT01045018
A BE Study Comparing Mesalamine 400 mg to ASACOL® 400 mg in Patients With Mild To Moderately Active Ulcerative Colitis
Collaborator
Lead: EMET Pharmaceuticals, LLC
Phase 3CompletedMild to Moderate Ulcerative Colitis2009-08