MedPath

PhaseBio Pharmaceuticals Inc

PhaseBio Pharmaceuticals Inc logo
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

14

Active:1
Completed:10

Trial Phases

2 Phases

Phase 1:8
Phase 2:6

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (14 trials with phase data)• Click on a phase to view related trials

Phase 1
8 (57.1%)
Phase 2
6 (42.9%)

Pemziviptadil (PB1046), a Long-acting, Sustained Release Human VIP Analogue, Intended to Provide Clinical Improvement to Hospitalized COVID-19 Patients at High Risk for Rapid Clinical Deterioration and Acute Respiratory Distress Syndrome (ARDS).

Phase 2
Terminated
Conditions
Respiratory Insufficiency
Pulmonary Inflammation
Respiratory Complication
Pneumonia
SARS-CoV-2
Coronavirus
Hypoxemic Respiratory Failure
Cardiac Infarct
Hypoxic Respiratory Failure
Pulmonary Edema
Interventions
Drug: Pemziviptadil (PB1046)
Drug: Low Dose (10 mg) Control
First Posted Date
2020-06-16
Last Posted Date
2020-12-11
Lead Sponsor
PhaseBio Pharmaceuticals Inc.
Target Recruit Count
54
Registration Number
NCT04433546
Locations
🇺🇸

Baptist Health Research Institute, Jacksonville, Florida, United States

🇺🇸

Sarasota Memorial Hospital, Sarasota, Florida, United States

🇺🇸

The University of Kansas Medical Center, Kansas City, Kansas, United States

and more 1 locations

Long-Term, Open Label Extension Study of Pemziviptadil (PB1046) in PAH Subjects Following Completion of Study PB1046-PT-CL-0004

Phase 2
Terminated
Conditions
Pulmonary Arterial Hypertension
Interventions
Drug: Pemziviptadil (PB1046) Injection
First Posted Date
2019-01-07
Last Posted Date
2022-02-22
Lead Sponsor
PhaseBio Pharmaceuticals Inc.
Target Recruit Count
25
Registration Number
NCT03795428
Locations
🇺🇸

University of California San Diego, La Jolla, California, United States

🇺🇸

University of California - Davis, Sacramento, California, United States

🇺🇸

University of Miami - Pulmonary Research Center, Miami, Florida, United States

and more 13 locations

Phase 2 Study to Assess Safety, Tolerability and Efficacy of Once Weekly SC Pemziviptadil (PB1046) in Subjects With Symptomatic PAH

Phase 2
Terminated
Conditions
Pulmonary Arterial Hypertension
Interventions
Drug: Pemziviptadil (PB1046)
First Posted Date
2018-06-14
Last Posted Date
2022-08-23
Lead Sponsor
PhaseBio Pharmaceuticals Inc.
Target Recruit Count
35
Registration Number
NCT03556020
Locations
🇺🇸

IMC - Diagnostic & Medical Clinic, LLC, Mobile, Alabama, United States

🇺🇸

Banner University Medical Center, Tucson, Arizona, United States

🇺🇸

University of California, San Diego (UCSD), La Jolla, California, United States

and more 23 locations

A Study to Assess the Safety, Tolerability, and Hemodynamic Response of PB1046 in Subjects With PAH

Phase 1
Completed
Conditions
Pulmonary Arterial Hypertension
Interventions
Drug: PB1046 Subcutaneous Injection
First Posted Date
2017-10-20
Last Posted Date
2019-10-08
Lead Sponsor
PhaseBio Pharmaceuticals Inc.
Target Recruit Count
3
Registration Number
NCT03315507
Locations
🇺🇸

The Ohio State University Wexner Medical Center, Columbus, Ohio, United States

🇺🇸

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States

Study to Assess the Safety, Tolerability and PK/PD After 4 Weekly SC Injections of PB1046 in Subjects With Stable HFrEF

Phase 2
Completed
Conditions
Heart Failure
Interventions
Drug: PB1046 Injection
Drug: Placebo Injection
First Posted Date
2016-06-22
Last Posted Date
2022-07-14
Lead Sponsor
PhaseBio Pharmaceuticals Inc.
Target Recruit Count
29
Registration Number
NCT02808585
Locations
🇺🇸

Pinnacle Research Group, LLC, Anniston, Alabama, United States

🇺🇸

Phoenix Medical Research, Peoria, Arizona, United States

🇺🇸

Cardiology Associates Research Company, Daytona Beach, Florida, United States

and more 2 locations
  • Prev
  • 1
  • 2
  • 3
  • Next

News

No news found

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.