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Study of Enfuvirtide in HIV-Positive Subjects

T

Trimeris

Status and phase

Completed
Phase 1

Conditions

AIDS
HIV Infections

Treatments

Drug: Fuzeon

Study type

Interventional

Funder types

Industry

Identifiers

NCT00086710
T20-405

Details and patient eligibility

About

A total of 26 patients will be admitted to the clinic where they will be dosed with each injection device. There will be a 7-day washout between doses and a 7-10 day follow-up period.

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Exclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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