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An Observational Study of Induction Therapy With Fuzeon (Enfuvirtide) in Combination With Antiretroviral Drugs in Patients With HIV-1 Infection

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Roche

Status

Completed

Conditions

HIV Infections

Study type

Observational

Funder types

Industry

Identifiers

NCT01902615
ML25313

Details and patient eligibility

About

This multicenter, retrospective, observational study will evaluate the therapeutic effectiveness of a strategy of induction with Fuzeon (enfuvirtide) within an optimized regimen of antiretroviral drugs in patients with HIV-1 infection in routine clinical practice.

Enrollment

58 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients, >/= 18 years of age
  • HIV-1+ infection
  • Patients with a viral load > 50 copies/ml who have received induction treatment with Fuzeon in combination with antiretroviral treatment
  • Naïve for Fuzeon at initiation of induction treatment
  • Antiretroviral treatment of at least 12 months duration

Exclusion criteria

  • Patients who did not receive Fuzeon treatment

Trial design

58 participants in 1 patient group

Cohort

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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