Current partner codePEPTIDESDE
NCT00086710·Phase 1·INTERVENTIONAL

Study of Enfuvirtide in HIV-Positive Subjects

Status

Completed

Phase

Phase 1

Enrollment

26

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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.

Interventions

Treatment arms and agents.

DRUG

Fuzeon

Timeline

From registration to results.

  1. First posted

    Jul 13, 2004

  2. Study start

    Not reported

  3. Primary completion

    Not reported

  4. Study completion

    Not reported

  5. Results posted

    Not reported

  6. Registry updated

    Jun 24, 2005

Outcomes

What the study measures.

Primary outcomes

Not reported in the indexed record.

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
64 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: \- Exclusion Criteria: \-

Study locations

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

SFBC

Miami, Florida, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Enfuvirtide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.