Status:
TERMINATED
An Extension Protocol for Virologically Suppressed Subjects Who Successfully Completed PRO140_CD03 Study
Lead Sponsor:
CytoDyn, Inc.
Conditions:
HIV-1-infection
Eligibility:
All Genders
18+ years
Phase:
PHASE2
PHASE3
Brief Summary
This study is a Phase 2b/3 multi-center extension study designed to evaluate the long term antiviral activity, safety, and tolerability of the strategy of continuing PRO 140 350mg, 525mg, or 700mg SC ...
Detailed Description
The objective is to assess the long-term safety of using PRO 140 350mg, 525mg, or 700mg SC as single-agent maintenance therapy for the chronic suppression of CCR5-tropic HIV-1 infection.
Eligibility Criteria
Inclusion
- Subjects who have completed 48 weeks of treatment in PRO140\_CD03 study.
- Last known Plasma HIV-1 RNA \< 50 copies/mL within PRO140\_CD03 study.
- Both male and female patients and their partners of childbearing potential must agree to use 2 medically accepted methods of contraception (e.g., barrier contraceptives \[male condom, female condom, or diaphragm with a spermicidal gel\], hormonal contraceptives \[implants, injectables, combination oral contraceptives, transdermal patches, or contraceptive rings\], and intrauterine devices) during the course of the study (excluding women who are not of childbearing potential and men who have been sterilized). Females of childbearing potential must have a negative serum pregnancy test at Screening visit and negative urine pregnancy test prior to receiving the first dose of study drug.
- Willing and able to participate in all aspects of the study, including use of SC medication, completion of subjective evaluations, attendance at scheduled clinic visits, and compliance with all protocol requirements as evidenced by providing written informed consent.
Exclusion
- Not currently enrolled in PRO140\_CD03 study.
- Any active infection or malignancy requiring acute therapy (with the exception of local cutaneous Kaposi's sarcoma).
- Females who are pregnant, lactating, or breastfeeding, or who plan to become pregnant during the study.
- Subjects weighing \< 35kg.
- History of anaphylaxis to any oral or parenteral drugs.
- History of Bleeding Disorder or patients on anti-coagulant therapy (except aspirin).
- Note: Subjects with well-controlled bleeding disorder while on stable anti-coagulant therapy dose with documented stable INRs can be enrolled as per discretion of the Investigator.
- Any other clinical condition that, in the Investigator's judgment, would potentially compromise study compliance or the ability to evaluate safety/efficacy.
Key Trial Info
Start Date :
August 29 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 10 2022
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT05271370
Start Date
August 29 2017
End Date
July 10 2022
Last Update
October 30 2025
Active Locations (1)
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1
Quest Clinical Research
San Francisco, California, United States, 94115