The Effects of r-metHuIFN-Gamma on the Lungs of Patients With AIDS
Launched by AMGEN · Aug 30, 2001
Trial Information
Current as of March 19, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- Patients must have:
- • Diagnosis of AIDS with one or more opportunistic infections.
- • Kaposi's sarcoma with prior history of opportunistic infection.
- • Stable dose of zidovudine (AZT) therapy.
- • Preserved pulmonary, renal and hepatic function.
- • Exclusion Criteria
- Co-existing Condition:
- Patients with the following conditions or symptoms are excluded:
- • Presence of active infection.
- • Active opportunistic infections.
- • Cardiac disease.
- • Central nervous system disorders.
- • History of seizures.
- • Irreversible airway disease.
- Patients with the following are excluded:
- • Co-existing conditions and symptoms listed in Patient Exclusion Co-existing Conditions.
- Prior Medication:
- Excluded within 4 weeks of study entry:
- • Immunosuppressive therapy.
- • Cytotoxic therapy.
- * Excluded:
- • Interferon gamma therapy.
About Amgen
Amgen is a leading global biotechnology company dedicated to discovering, developing, manufacturing, and delivering innovative human therapeutics. With a strong focus on areas such as oncology, cardiovascular disease, and inflammation, Amgen leverages advanced science and technology to address complex medical needs. The company is committed to improving patient outcomes through rigorous clinical trials and robust research initiatives, ensuring the highest standards of safety and efficacy in its products. With a rich pipeline of cutting-edge therapies, Amgen continues to be at the forefront of biopharmaceutical advancements, making a significant impact on healthcare worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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