Safety and Impact of Baricitinib on Cell Surivival Pathways, HIV-1 Reservoir and Inflamation in People With HIV-1

NCT ID: NCT07028385

Last Updated: 2025-12-01

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-22
• Study Completion Date: 2026-04-30

Brief Summary

The goal of this exploratory clinical trial is to evaluate the safety and tolerability of bariticinib administered at 2 mg once daily during 12 weeks in 30 people living with HIV-1 (PWH) on suppressive antiretroviral therapy (ART) and to evaluate changes in levels of phosphorylated STAT (pSTAT) after 12 weeks of treatment with bariticinib. The main questions it aims to answer are:

• The safety and tolerability of bariticinib
• To evaluate the effects of bariticinib on T-cells (HIV-1 reservoirs, apoptosis, inflamation, activation and exhaustion).
• To characterize bariticinib pharmacokinetics in plasma.

Participants will be treated with pral Barticinib 2mg or matched Placebo daily for 12 weeks. Suppressive cART will remain unchanged during the entire study. Participants will be followed until week 24, in a total of 8 visits.

Detailed Description

Despite the success of antiretroviral therapy (ART) in suppressing HIV replication, it does not eliminate the latent viral reservoir, which remains a major barrier to achieving a cure. Recent evidence suggests that HIV-infected cells may evade immune clearance by overexpressing anti-apoptotic proteins such as BCL-2, contributing to reservoir persistence. Baricitinib, a second-generation Janus kinase (JAK) inhibitor has shown potential in preclinical studies to reduce HIV reactivation and modulate immune activation.

This study investigates whether baricitinib can safely modulate the HIV-1 reservoir and immune environment in PWH on suppressive ART.

Participants will be randomized (2:1) to receive either oral baricitinib 2 mg or placebo daily for 12 weeks, followed by a 12-week observation period.

The primary objectives are to assess the safety and tolerability of baricitinib and to evaluate changes in phosphorylated STAT (pSTAT) levels in CD4+ T cells as a pharmacodynamic marker.

Secondary objectives include evaluating the effects of baricitinib on BCL-2 expression, JAK/STAT signaling, HIV-1 reservoir size, inflammatory biomarkers, and immune cell subsets.

Exploratory analyses will assess HIV-specific T cell responses, CD4+ T cell susceptibility to cytotoxic T lymphocyte (CTL) killing, and transcriptomic changes.

Conditions

HIV

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Bariticinib

Participants will take one capsule containing 2 mg of baricitinib, once daily, oral administration for 12 weeks

Group Type: EXPERIMENTAL

Bariticinib 2 mg

Intervention Type: DRUG

Commercially available tablets containing 2 mg of barticiinib will be used. The tablets will be re-capsulated to keep the study blind.

Placebo

Participants will take one capsule containing inert substance (maltodextrine), once daily, oral administration for 12 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Maltodextrin capsules with identical weight and appearance (shape, size, colour and flavour) as the bariticinib-containing capsules.

Interventions

Bariticinib 2 mg

Commercially available tablets containing 2 mg of barticiinib will be used. The tablets will be re-capsulated to keep the study blind.

Intervention Type: DRUG

Placebo

Maltodextrin capsules with identical weight and appearance (shape, size, colour and flavour) as the bariticinib-containing capsules.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Males and females aged between 18 and 65 years on the day of screening visit.
• Confirmed HIV-1 infection.
• Receiving suppressive cART for at least 2 years (defined as maintained plasma viral load <50 copies/mL, allowing for isolated blips [<200 cop/ml, non-consecutive, representing <20% total determinations]).
• Being on the same cART regimen within at least 4 weeks prior to baseline visit (week 0).
• Willing and able to be adherent to their cART regimen for the duration of the study.
• Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the study.
• In the opinion of the clinical Investigator, the candidate has understood the information provided and can give written Informed Consent.
• If heterosexually active female of childbearing potential using an effective method of contraception different from hormonal contraception (intra-uterine device (IUD), anatomical sterility in self or partner or sexual abstinence) from 14 days prior to the first IMP administration and commit to use it until 3 months after the last IMP administration. All female candidates of childbearing potential who are not sexually active with men at screening, must agree to utilize an effective method of contraception if they become sexually active during the study.
• If female of childbearing potential, willing to undergo urine pregnancy tests at the designated time points.
• If positive IgG for varicella zoster, adequate herpes zoster vaccination at least 4 weeks prior to week 0 visit.
• Willing to accept blood draws at time points specified in the Schedule of Events.

Exclusion Criteria

• If female of childbearing potential, pregnant or planning a pregnancy during the entire study or lactating.
• Prior history or clinical manifestations of any physical or psychiatric disorder that could impair the subject's ability to complete the study.
• Any active AIDS-defining disease or progression of HIV-related disease, except cutaneous Kaposi's sarcoma not requiring systemic therapy.
• Ongoing malignancy other than cutaneous Kaposi's sarcoma, basal cell carcinoma, or resected, non-invasive cutaneous squamous cell carcinoma, or cervical, anal, or penile intraepithelial neoplasia.
• Systemic treatment for cancer within 1 year of study entry.
• Known hypersensitivity to any component of the IMP formulation, or severe or multiple allergies to drugs or pharmaceutical agents.
• Potential participant received or plans to receive:

i. Licensed live attenuated vaccines within 28 days before or after inflammation and immune biomarkers visit (weeks 0 and 12).

ii. Other vaccines (eg, tetanus, hepatitis A, hepatitis B, rabies, pneumococcal, recombinant Herpes Zoster, Influenza, COVID-19 vaccines) within 14 days before or after inflammation and immune biomarkers visits (weeks 0 and 12).

• Receipt of blood products within 3 months of study entry.
• Current or recent use (within last 3 months) of interferon or systemic corticosteroids or other immunosuppressive agents (use on inhaled steroids for asthma or topic steroids for localized skin conditions are permitted).
• Any other current or prior therapy which, in the opinion of the investigator, would make the individual unsuitable for the study or influence the results of the study.
• Prior history of thrombotic events (deep venous thrombosis, pulmonary embolism, or arterial thrombosis) or known inherited prothrombotic disorders (Factor V Leiden, prothrombin G2021A mutation, antithrombin deficiency, protein S deficiency, protein C deficiency, etc).
• Current use of combined hormonal contraceptives or substitutive hormonal treatment.
• History of any of the following cardiovascular diseases: myocardial infarction, unstable angina, congestive heart failure, uncontrolled arrhythmias, cardiac revascularization, stroke, uncontrolled hypertension, or uncontrolled diabetes within 6 months.
• Current smokers over 10 cigarettes per day or former smokers with a history of smoking more than 10 packyears, unless they quit smoking more than 15 years ago.
• Positive hepatitis C IgG, unless confirmed clearance of HCV infection (undetectable plasma viral load, spontaneous or following treatment).
• Chronic hepatitis B, defined as positive hepatitis B surface antigen (HBsAg); or past hepatitis B, defined as positive hepatitis B core antibody (HBcAb), unless ART regimen contains FTC/TFV during the study.
• Symptomatic herpes zoster or recurrent genital herpes within 24 weeks, or any history of disseminated herpes simplex, disseminated herpes zoster, ophthalmic zoster, or CNS zoster.
• History of active, past, or latent tuberculosis, confirmed through medical history, clinical records, or a positive TB IGRAs by QuantiFERON test, unless documented preventive TB treatment with 6 or 9 months of daily isoniazid, or a 3-month regimen of weekly rifapentine plus isoniazid, or a 3-month regimen of daily isoniazid plus rifampicin.
• Any laboratory abnormalities including:

Hematology

• Hemoglobin <10.0 g/dl,
• Absolute neutrophil count ≤1,000 /mm3,
• Absolute lymphocyte count ≤500 /mm3,
• Platelets >450,000/mm3, Biochemistry
• eGFR <30 ml/min,
• AST > 2.5 x ULN,
• ALT > 2.5 x ULN,

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

IrsiCaixa

OTHER

Sponsor Role: collaborator

University of Turin, Italy

OTHER

Sponsor Role: collaborator

Instituto de Salud Carlos III

OTHER_GOV

Sponsor Role: collaborator

Germans Trias i Pujol Hospital

OTHER

Sponsor Role: collaborator

Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Fundació Lluita contra les Infeccions - Hospital Universitari Germans Trias i Pujol

Badalona, Barcelona, Spain

Site Status: RECRUITING

Countries

Spain

Central Contacts

José Moltó, MD, PhD

Role: CONTACT

jmolto@lluita.org

+34934657897

David Rovira

Role: CONTACT

drovira@scienhub.org

+34934978849

Facility Contacts

Fundacion Fls De Lucha Contra El Sida

Role: primary

info@fls-rs.com

+34934978414

Other Identifiers

BCN05-Bari

Identifier Type: -

Identifier Source: org_study_id

2024-520159-26-00

Identifier Type: CTIS

Identifier Source: secondary_id