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The Wistar Institute

The Wistar Institute logo
🇺🇸United States
Ownership
Private
Established
1972-01-01
Employees
501
Market Cap
-
Website
http://www.wistar.org

Clinical Trials

5

Active:0
Completed:4

Trial Phases

3 Phases

Phase 1:1
Phase 2:3
Not Applicable:1

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 (5 trials with phase data)• Click on a phase to view related trials

Phase 2
3 (60.0%)
Not Applicable
1 (20.0%)
Phase 1
1 (20.0%)

Reducing Proviral HIV DNA With Interferon-a

Phase 2
Conditions
HIV
HIV/AIDS
Interventions
Drug: Peg-IFN-α2b
First Posted Date
2014-08-28
Last Posted Date
2018-04-05
Lead Sponsor
The Wistar Institute
Target Recruit Count
54
Registration Number
NCT02227277
Locations
🇺🇸

Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

🇺🇸

Penn-Presbyterian Hospital, Philadelphia, Pennsylvania, United States

🇺🇸

Jonathan Lax Center at Philadelphia FIGHT, Philadelphia, Pennsylvania, United States

Pilot Peg-Interferon-a2b in Decreasing Viral DNA in HIV

Phase 2
Completed
Conditions
HIV-1 Infection
Interventions
Drug: Pegylated Interferon alpha 2b
First Posted Date
2013-09-04
Last Posted Date
2023-07-06
Lead Sponsor
The Wistar Institute
Target Recruit Count
20
Registration Number
NCT01935089
Locations
🇺🇸

AIDS Clinical Trials Unit (ACTU), and Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States

🇺🇸

Presbyterian Hospital, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States

🇺🇸

Jonathan Lax Clinic, Philadelphia FIGHT, Philadelphia, Pennsylvania, United States

Antiviral Activity of Peg-IFN-Alpha-2A in Chronic HIV-1 Infection

Phase 2
Completed
Conditions
HIV Infections
Interventions
Drug: Pegylated Interferon-alpha 2a, 180 mcg/week sc
Drug: Pegylated Interferon-alpha 2a, 90 mcg/week sc
First Posted Date
2008-01-16
Last Posted Date
2015-02-10
Lead Sponsor
The Wistar Institute
Target Recruit Count
23
Registration Number
NCT00594880
Locations
🇺🇸

Drexel University College of Medicine, Philadelphia, Pennsylvania, United States

🇺🇸

Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

🇺🇸

Penn-Presbyterian Medical Center, Philadelphia, Pennsylvania, United States

and more 2 locations

Anti-HIV Treatment Interruptions in HIV Infected Adults in South Africa

Not Applicable
Completed
Conditions
HIV Infections
Interventions
Behavioral: Structured treatment interruption
Biological: Rabies de novo antigen
First Posted Date
2005-01-05
Last Posted Date
2014-08-27
Lead Sponsor
The Wistar Institute
Target Recruit Count
30
Registration Number
NCT00100646
Locations
🇿🇦

University of the Witwatersrand, Johannesburg, South Africa

Immune and Viral Outcomes of HIV-1 Therapy Interruption

Phase 1
Completed
Conditions
HIV Infections
First Posted Date
2003-01-24
Last Posted Date
2016-02-09
Lead Sponsor
The Wistar Institute
Target Recruit Count
20
Registration Number
NCT00051818
Locations
🇺🇸

The Wistar Institute, Philadelphia, Pennsylvania, United States

News

Wistar Institute Launches $17 Million Personalized HIV Cure Initiative with Six-Component Therapy Approach

The Wistar Institute received a five-year, $17 million NIH grant to launch the iCure Consortium, developing individualized cure regimens for HIV through personalized medicine approaches.

Wistar Institute Scientists Develop Next-Generation DNA-LNP Vaccine Technology with Enhanced Immune Response

Scientists at The Wistar Institute, University of Pennsylvania, and INOVIO have successfully combined plasmid DNA with lipid nanoparticle delivery systems, overcoming previous stability and efficacy challenges.

INOVIO's DNA-Encoded Monoclonal Antibodies Show Durable 72-Week Expression Without Immune Rejection in COVID-19 Trial

INOVIO's Phase 1 trial demonstrates DNA-encoded monoclonal antibodies (DMAbs) maintained stable levels for 72 weeks in all participants, potentially overcoming the short half-life limitations of traditional antibody therapies.

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