A Clinical Trial of STP0404 in Adults with HIV-1 Infection

Description

The purpose of this study is to evaluate the antiviral effect, safety, tolerability, and pharmacokinetics of STP0404 in adult participants living with Human Immunodeficiency Virus Type 1 (HIV-1) infection.

Conditions

HIV-1-infection

Study Overview

Study Details

Study overview

The purpose of this study is to evaluate the antiviral effect, safety, tolerability, and pharmacokinetics of STP0404 in adult participants living with Human Immunodeficiency Virus Type 1 (HIV-1) infection.

A Phase 2a, Randomized, Double-Blinded, Placebo-Controlled, Multicenter Study to Investigate the Antiviral Effect, Safety, Tolerability, and Pharmacokinetics of STP0404 in Adults with HIV-1 Infection

A Clinical Trial of STP0404 in Adults with HIV-1 Infection

Condition
HIV-1-infection
Intervention / Treatment

-

Contacts and Locations

Los Angeles

Kaiser Permenente Los Angeles Medical Center, Los Angeles, California, United States, 90027

Los Angeles

Ruane Clinical Research, Inc., Los Angeles, California, United States, 90036

Fort Pierce

Midway Immunology and Research Center, Fort Pierce, Florida, United States, 34982

Miami

Schiff Center for Liver Diseases/University of Miami, Miami, Florida, United States, 33136-2107

Orlando

Orlando Immunology Center, Orlando, Florida, United States, 32803

Tampa

USF Health South Tampa Center for Advanced Healthcare, Tampa, Florida, United States, 33602-3511

Berkley

Be Well Medical Center, Berkley, Michigan, United States, 48072

Newark

Saint Michael's Medical Center, Newark, New Jersey, United States, 07102

Somers Point

South Jersey Infectious Disease, Somers Point, New Jersey, United States, 08244

Manhasset

North Shore University Hospital, Manhasset, New York, United States, 11030-3816

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Have a confirmed HIV-1 infection in the documented medical record or at screening.
  • * Have never received any ARTs (i.e., treatment-naïve) before screening or only received one ARV regimen (2 or 3 drugs) at least 12 weeks before screening and/or received any monotherapy ≤10 days in a clinical trial setting at least 12 weeks before screening. Participants with a documented history of PrEP and/or PEP therapy but discontinued at least 8 weeks prior to screening are also eligible for inclusion.
  • * Have a CD4+ cell count ≥200 cells/mm3 at screening.
  • * Have a hepatitis B surface antigen or positive hepatitis C virus antibody at screening. An HCV confirmation (HCV RNA test) will be performed at a central laboratory if the HCV antibodies screening result is positive. If the HCV RNA test result is negative, the participant will be eligible.
  • * Have a positive drug screen for amphetamines, barbiturates, cocaine, opiates, benzodiazepines, heroin, or phencyclidine. However, if in the opinion of the investigator, positive drug screen results may be due to prescription medication for therapeutic purposes (e.g., prescription Adderall for ADHD), eligibility decision shall rely on the investigator's medical judgment and should be documented.
  • * Have a history of regular alcohol consumption, defined as an average weekly intake of \>14 drinks (males) or \>7 drinks (females), within 6 months of screening and/or has positive alcohol screen at screening and baseline.
  • * Have received the following treatments as PrEP or PEP (≥1 dose) prior to screening: monoclonal antibodies, HIV-1 maturation inhibitors, and long-acting INSTIs (such as cabotegravir).
  • * Pregnant or lactating females.
  • * Have a history of clinically relevant pancreatitis or hepatitis within the previous 6 months.
  • * Participant received any allosteric HIV-1 integrase inhibitor (ALLINI, ≥1 dose) and/or received any long-acting ARVs (marketed or investigational, ≥1 dose) prior to screening.
  • * Have previously failed an INSTIs-containing regimen.

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

ST Pharm Co., Ltd.,

Study Record Dates

2025-12-31