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Approved for marketingNCT00377065Updated Apr 22, 2016

Early Access of MK0518 in Combination With an Optimized Background Antiretroviral Therapy (0518-023)

An expanded access record providing raltegravir in HIV Infections, sponsored by Merck Sharp & Dohme LLC. Approved for marketing. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2016-04-22.

Sponsored by Merck Sharp & Dohme LLC · Expanded access

Study type
Expanded access
Ages
16 Years and older
Sex
All
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Study summary

This is a treatment use study to provide early access to MK0518 for the treatment of HIV-1 infection in patients who have limited or no treatment options due to virological failure, resistance, or intolerance to multiple antiretroviral regimens. Enrollment in this study is patient driven. Investigators are not proactively assigned. There is no target sample size and duration of the study is indefinite. For information on how to enroll in the study, see link below.

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Conditions studied

  • HIV Infections

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03

In context

HIV Infections

4,258 studies on the registry are indexed under HIV Infections; 240 are open to participants now.

Browse HIV Infections studies →

Lead sponsor

Merck Sharp & Dohme LLC is the lead sponsor of 2,114 studies on the registry; 133 are open to participants now.

Of its 489 completed or terminated interventional studies of FDA-regulated products, 362 (74%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • HIV positive patients who have limited or no treatment options and have documented resistance

Exclusion criteria

Exclusion Criteria:

  • Patient has previously been on MK0518 therapy
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Access details

Study type
Expanded access

Available treatment

  • Drugraltegravir

    raltegravir 400 mg P.O. bid tablet twice daily for 12 weeks

    Also known as: MK0518, ISENTRESS™

06

Where to request access

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 22, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00377065
Lead sponsor
Merck Sharp & Dohme LLC
Responsible party
Sponsor
First posted
Sep 15, 2006
Last update
Apr 22, 2016

Study contacts

Medical Monitor
study director · Merck Sharp & Dohme LLC
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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