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The HIV Functional Cure Potential of UB-421 in ART Stabilized HIV-1 Patients

U

United BioPharma

Status and phase

Completed
Phase 2

Conditions

HIV-1 Infection

Treatments

Biological: UB-421(25 mg/kg) Q4W
Biological: UB-421(25 mg/kg) Q2W

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03743376
UBP-A209-HIV

Details and patient eligibility

About

This study evaluate the safety of UB-421 in combination with standard antiretroviral therapy (ART) and the efficacy of HIV reservoir reduction as compared with ART alone in ART stabilized HIV-1 patients

Enrollment

31 patients

Sex

All

Ages

20 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. HIV-1 sero-positive
  2. Male with body weight ≥ 50 kg or female with body weight ≥ 45 kg.
  3. HIV-1 plasma RNA level below 50 RNA copies/mL .

Exclusion criteria

  1. Subjects with active systemic infections, except for HIV-1, that the Investigator feels the infections may confound evaluation and treatment for HIV-1.
  2. Current active hepatitis B carriers, ie, hepatitis B surface antigen positive.
  3. Current active hepatitis C carriers, ie, hepatitis C virus (HCV) antibody positive.
  4. History of anaphylaxis to other mAbs.
  5. Any vaccination within 8 weeks prior to the first dose of assigned drug.
  6. Use of immunomodulators, HIV vaccine, or systemic chemotherapy within 180 days prior to the first dose of assigned drug.
  7. Females who are pregnant, lactating, or breastfeeding, or who plan to become pregnant during the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

31 participants in 3 patient groups

Standard ART
No Intervention group
Description:
Subjects will receive standard ART for 48 weeks
UB-421(25mg/kg) Q2W add-on treatment
Experimental group
Description:
UB-421(25 mg/kg) Q2W plus standard ART for 48 weeks
Treatment:
Biological: UB-421(25 mg/kg) Q2W
UB-421(25mg/kg) Q4W add-on treatment
Experimental group
Description:
UB-421(25 mg/kg) Q4W plus standard ART for 48 weeks
Treatment:
Biological: UB-421(25 mg/kg) Q4W

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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