Study of Safety and Pharmacokinetics in Healthy Volunteers and Safety, Tolerability and Antiviral Activity of VM-1500 in Patients With Human Immunodeficiency Virus-1 Infection

Viriom

Status and phase: Completed; Phase 2; Phase 1

Conditions: HIV Infection

Treatments: Drug: VM-1500/Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT02485509

VM-1500-001

Details and patient eligibility

About

A combined Phase Ib and IIa randomized, placebo-controlled, double-blind study of VM-1500 in healthy subjects and in patients with HIV-1 infection that are antiretroviral therapy naïve.

Full description

The study will be split into two parts:

Part I: A randomized, placebo-controlled, single dose, double-blind study in healthy volunteers with 20 mg followed by 40 mg after DSMB approval.

Healthy group: one dose with 1 PK day 12 health volunteers (total): 6 subjects will randomized (4:2) to VM-1500 20 mg or placebo. After DSMB approval, 6 subjects will be randomized (4:2) to VM-1500 40 mg or placebo Part II: A randomized, placebo-controlled, multiple dose, double-blind study for 7 days in patients with HIV infection who are antiretroviral therapy-naïve. After positive DMSB review the dose will be escalated from 20 mg to 40 mg once daily.

Patient group: 2 PK days (in-house) at day 1 and day 7 16 patients (total): 8 subjects will be randomized (7:1) to VM-1500 20 mg or placebo once daily for 7 days. After DSMB approval, 8 subjects will be randomized (7:1) to VM-1500 40 mg or placebo once daily for 7 days.

Enrollment: 28 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Healthy Subjects:

1. Male age between 18-40 years

2. Has been determined healthy by physical examination, assessment of drug abuse, medical history and vital signs

3. Has normal results for the following screening tests: complete blood count , blood urea nitrogen, serum creatinine , fasting blood sugar, total bilirubin, aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase and urinalysis.

4. Negative result for hepatitis B, hepatitis C and HIV antibodies

5. Willing to participate and signed the informed consent form

   Inclusion Criteria for Patients:

6. Males or females aged 18 to 65 years

7. HIV-1 infection, as documented by a rapid HIV test or any licensed ELISA test kit and confirmed by Western blot at any time prior to study entry

8. Antiretroviral therapy naïve.

Exclusion Criteria for Healthy Subjects:

1. Hepatic or kidney disorders or any other disease or disorder which may in the opinion of the Investigator interfere with the results of the study or threaten the health of volunteers;
2. Drug intake (including herbal drugs) during the last month;
3. Active alcohol or and/or drug abuse that, in the opinion of the site investigator, would interfere with adherence to study requirements;
4. Volunteers have taken any investigational drug at least 3 month prior to the start of the study;
5. Inability to understand the Protocol or follow its instructions;

Exclusion Criteria for Patients:

1. Currently has any active AIDS defining illness
2. Exclusionary resistance mutations defined as evidence of any major NNRTI mutations according to the current IAS list of HIV-1 Resistance Mutations Associated with Drug Resistance on any genotype; or evidence of significant NNRTI resistance on any phenotype performed at any time prior to study entry.
3. Patients who are expected to need systemic antiviral therapy at any time during their participation in the study.
4. Patients who have received an investigational drug for HIV, HIV vaccine, immunomodulators, systemic cytotoxic chemotherapy, or other investigational therapy within 30 days prior to study entry;
5. Acute or chronic viral hepatitis;
6. History or other evidence of renal disease.
7. Abnormal hematological and biochemical parameters within 30 days of Entry (Day 1).
8. Screening ECG QTc value 450 ms.
9. Consumption / administration of concomitant medication.
10. Active alcohol and/or drug abuse that, in the opinion of the site investigator, would interfere with adherence to study requirements.
11. Positive results on urine screen for drugs of abuse at Screening or Day 1
12. History of immunologically mediated disease.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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28 participants in 4 patient groups

20 mg VM-1500/Placebo Healthy group

Experimental group

Description:

VM-1500 20 mg or placebo single dose.

Treatment:

Drug: VM-1500/Placebo

40 mg VM-1500/Placebo Healthy group

Experimental group

Description:

VM-1500 40 mg or placebo single dose.

Treatment:

Drug: VM-1500/Placebo

20 mg VM-1500/Placebo Patient group

Experimental group

Description:

VM-1500 20 mg or placebo once daily for 7 days.

Treatment:

Drug: VM-1500/Placebo

40 mg VM-1500/Placebo Patient group

Experimental group

Description:

VM-1500 40 mg or placebo once daily for 7 days.

Treatment:

Drug: VM-1500/Placebo