Actively Recruiting

Phase 2
Age: 18Years - 65Years
All Genders
NCT05527418

Safety, Tolerance and Antiretroviral Activity of Dasatinib: a Pilot Clinical Trial in Patients With Recent HIV-1 Infection

Led by Eva Bonfill · Updated on 2025-05-01

24

Participants Needed

1

Research Sites

122 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Study to evaluate the safety, tolerability and antiretroviral activity of a new therapeutic strategy, based on the administration of dasatinib, an ITK, in patients with recent (3-12 months) asymptomatic HIV-1 infection.

CONDITIONS

Official Title

Safety, Tolerance and Antiretroviral Activity of Dasatinib: a Pilot Clinical Trial in Patients With Recent HIV-1 Infection

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 65 years
  • Documented asymptomatic HIV-1 infection lasting 3 to 12 months with positive Western blot including p31 band
  • No prior antiretroviral therapy
  • CD4 T-lymphocyte count greater than 350 cells per microliter
  • Able and willing to provide written informed consent
Not Eligible

You will not qualify if you...

  • Active hepatitis B (HBsAg+ or DNA+) or hepatitis C (RNA+) infection at screening
  • ALT greater than twice the upper normal limit
  • Glomerular filtration rate less than 70 mL/1.73 m2
  • Leukocytes fewer than 4000/mm3
  • Total lymphocyte count fewer than 1000/mm3
  • Platelet count fewer than 100,000/mm3
  • Hemoglobin less than 12 g/dL
  • Pregnancy or active breastfeeding
  • History or presence of pleural effusion
  • Chronic obstructive pulmonary disease, bronchial asthma, or recent chest trauma
  • History of gastrointestinal or other bleeding
  • Current use of drugs that may dangerously interact with dasatinib
  • Any clinical condition judged by the investigator to contraindicate participation, including active cancer or active infection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Eva Bonfill

Barcelona, Spain

Actively Recruiting

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Research Team

E

Eva Bonfill

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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