Safety, PK and PD Study of ABX464 in Untreated HIV Patients

Phase 2

Completed

• Conditions: Human Immunodeficiency Virus Infections
• Interventions: Other: Placebo; Drug: ABX464

• Registration Number: NCT02452242
• Lead Sponsor: Abivax S.A.

Brief Summary

ABX464 is a first in class that showed efficacy as an anti-HIV therapy. The present study is intended to assess the safety, the tolerability, and pharmacokinetic parameters and to evaluate the effect on viral load of repeated oral administrations of ABX464 in patients infected by HIV, not previously treated for their HIV.

Two types of design are intended in this protocol: dosing every 3 days or dosing every day. The goal is to determine the best dosing regimen to reduce viral load and minimize adverse events.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01
• Study First Submitted: 2015-04-10
• Status Verified: 2015-05
• Study First Submitted QC: 2015-05-20
• Study First Posted: 2015-05-22
• Primary Completion: 2015-12
• Study Completion: 2016-05
• Last Update Submitted: 2016-05-27
• Last Update Posted: 2016-05-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

1. Males or females, 18 to 65 years of age
2. Patients infected by HIV-1 or HIV-2
3. BMI between 17 and 29 kg/m².
4. CD4 cell count ≥ 350 /mm3 and HIV RNA level between 5,000-500,000 copies/mL.
5. Clinical laboratory tests (hematology, blood chemistry, and urinalyses) must be within normal limits, or clinically acceptable to the sponsor and principal investigator and consistent with the underlying HIV infection.
6. Urine drug screen for drugs with a high potential for abuse (cocaine, opiates, amphetamines and barbiturates) and alcohol breath test must be negative.
7. Females must be non lactating and either be of nonchildbearing potential (ie sterilized via hysterectomy or bilateral tubal ligation or at least one year post-menopausal) or if of child bearing potential, must be practicing effective double barrier contraceptive methods from at least two weeks prior to Day 1 until 3 months after the last dose of study medication.
8. Males must practice an effective barrier method of contraception from Day 1 until 3 months days after the last dose of study medication.
9. Patients must be willing to give written informed consent prior to study enrollment and be able to adhere to restrictions and examination schedules.
10. Physical examination and ECG must be within normal limits.
11. Never taken any antiretroviral agent except for a brief time, and for some reasons, the patient decided not to continue therapy (i.e. Toxicity, personal decision. None in past 30-180 days.

Exclusion Criteria

1. Individuals with a history of any significant medical disorders which requires a physician's care.
2. Individuals who have a history of any clinically significant local or systemic infectious disease (other than HIV-1 or HIV-2 infection) within four weeks prior to drug administration.
3. Individuals with any clinically significant laboratory abnormalities as defined as grade 2 or 3 in Common Terminology Criteria for Adverse Events (CTCAE), version 4.0.
4. Individuals who are positive for hepatitis B virus and/or hepatitis C virus
5. Any individual who does not comply with the requirement that he should not have used any drugs (including prescription, nonprescription, herbal, and mineral supplements) other than paracetamol for at least two weeks prior to the study nor alcohol within 48 hours prior to drug administration and for the entire study period. The use of a concomitant medications to treat an AE during the study will not be considered a protocol violation.
6. Individuals who have participated in a clinical trial of an investigational drug within 90 days prior to the start of the study
7. Individuals who smoke more than ten cigarettes or equivalent tobacco use per day.
8. Individuals with forfeiture of freedom by an administrative or legal obligation or under guardianship

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	-
ABX464	ABX464	-

Primary Outcome Measures

Name	Time	Method
Safety and tolerability profile of ABX464 as assessed by the change from baseline in laboratory values, in vital signs and ECG parameters at week 3 and by the number of patients with adverse events.	Week 3	Number of patients with abnormal blood (hematology and biochemistry) and urinary laboratory values, abnormal vital signs and ECG parameters and the number/proportion of patients reporting any adverse event.

Secondary Outcome Measures

Name	Time	Method
t1/2	Week 3	Half-life of the ABX464 in plasma
tmax	Week 3	Time to maximum concentration
Pharmacodynamic activity as expressed by CD4 and CD8 count	Week 3	CD4 and CD8 values
Pharmacodynamic activity as expressed by HIV viral load	Week 3	HIV viral load across time and possible relationship with PK parameters
Cmax	week 1, week 2 and week 3	Maximum concentration in plasma of ABX464 and metabolite
AUC	Week 3	Area under the concentration-time curve

Trial Locations

Locations (4)

CAP Research Ltd; 🇲🇺 Curepipe, Mauritius

Chiang Mai University; 🇹🇭 Chiang Mai, Thailand

Siriraj Hospital, Mahidol University; 🇹🇭 Bangkok, Thailand

HIV-NAT, Thai Red Cross AIDS Research Center; 🇹🇭 Bangkok, Thailand