Home » Drug Information » FDA-Approved Drugs » 2003
Medical Areas: Immunology/Infectious Diseases
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Drug Information
The following information is obtained from various newswires, published
medical journal articles, and medical conference presentations.
Company: Trimeris, Roche
Approval Status: Approved March 2003
Treatment Area: HIV Infection
Fuzeon (enfuvirtide) is an HIV (human immunodeficiency virus)
fusion inhibitor that helps block the viruses ability to infect
healthy T- cells. Fuzeon does not lower the chance of passing HIV
to other people through unprotected sex, sharing needles or being
exposed to blood. This drug does not does not cure HIV infection or
AIDS and must be taken as part of a combination antiretroviral
regimen.
Fuzeon in combination with other antiretroviral agents is
indicated for the treatment of HIV-1 infection in
treatment-experienced patients with evidence of HIV-1 replication
despite ongoing antiretroviral therapy.
The drug is given under the skin by injection in the upper arm,
upper leg or stomach two times a day. The recommended dose of is 90
mg (1 mL) twice daily
FDA approval of Fuzeon was based on data from two 24-week phase
III pivotal studies of approximately 1,000 subjects, TORO 1
(T20-301), conducted in North America and Brazil, and TORO 2
(T20-302), conducted in Europe and Australia. These studies showed
that treatment-experienced subjects receiving Fuzeon as a part
combination regimen of anti-HIV drugs, experienced greater
immunologic improvements and were twice as likely to achieve
undetectable plasma levels of HIV compared to subjects receiving a
anti-HIV regimen alone. In addition, those subjects with two or
more active drugs in their background regimen were more likely to
achieve undetectable levels of HIV.
Studies T20-301 and T20-302 are ongoing, randomized, controlled,
open label, multicenter trials in HIV-1 infected subjects. Subjects
were required to have either (1) viremia despite 3 to 6 months
prior therapy with a nucleoside reverse transcriptase inhibitor
(NRTI), non-nucleoside reverse transcriptase inhibitor (NNRTI), and
protease inhibitor (PI) or (2) viremia and documented resistance or
intolerance to at least one member in each of the NRTI, NNRTI, and
PI classes.
Adverse events associated with the use of Fuzeon may include
(but are not limited to) the following:
- Local injection site reaction
- Pain and discomfort
- Induration
- Erythema
- Nodules and cysts
- Pruritus
- Ecchymosis
- Diarrhea
- Conjunctivitis
- Pancreatitis
Fuzeon blocks HIV’s ability to infect healthy CD4 cells. When
used with other anti- HIV medicines, Fuzeon can reduce the amount
of HIV in the blood and increase the number of CD4 cells. This may
keep the immune system healthy, so it can help fight infection.
The active ingredient, enfuvirtide, interferes with the entry of
HIV-1 into cells by inhibiting fusion of viral and cellular
membranes. Enfuvirtide binds to the first heptad-repeat (HR1) in
the gp41 subunit of the viral envelope glycoprotein and prevents
the conformational changes required for the fusion of viral and
cellular membranes.
Ball RA et al. Pathology of injection site
reactions with enfuvirtide. Tenth Conference on Retroviruses
and Opportunistic Infections, Boston, abstract P714, 2003.
Boyd M et al. Enfuvirtide: investigations on
the drug interaction potential in HIV-infected patients. Tenth
Conference on Retroviruses and Opportunistic Infections,
Boston, abstract P541, 2003.
Church J et al. Safety and antiretroviral
activity of chronic subcutaneous administration of T-20 in human
immunodeficiency virus 1-infected children. Pediatric
Infectious Disease Journal 21(7):653-659, 2002.
Greenberg ML et al. Baseline and on-treatment
susceptibility to enfuvirtide seen in TORO 1 and TORO 2 to 24
weeks. Tenth Conference on Retroviruses and Opportunistic
Infections, Boston, abstract 141, 2003.
Heil M et al. Analysis of patient-derived HIV-1
isolates suggests a novel mechanism for decreased sensitivity to
inhibition by enfuvirtide and T-649. Tenth Conference on
Retroviruses and Opportunistic Infections, Boston, abstract
615, 2003.
Sista P et al. The fusion inhibitors T-20 and
T-1249 demonstrate potent in vitro antiviral activity against clade
B HIV-1 isolates resistant to reverse transcriptase and protease
inhibitors and non-B clades. Antiviral Therapy
6(Supplement 1):3, 2001.