Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of aldesleukin (recombinant interleukin-2), zidovudine (an NRTI), and ganciclovir (an antiviral). It was evaluated by the AIDS Malignancy Consortium (AMC) in the Phase II pilot study AMC 019 for the treatment of AIDS-related primary central nervous system lymphoma (PCNSL). Aldesleukin acts as an immunomodulatory biologic agent that functions as a T-cell growth factor to enhance immune function in profoundly immunosuppressed patients. Zidovudine and ganciclovir are included to target the underlying viral drivers of the malignancy, specifically HIV and Epstein-Barr virus (EBV), which is consistently associated with AIDS-related PCNSL. The regimen was designed as both induction and maintenance therapy to address both the immune dysfunction and the viral etiology of this rare B-cell lymphoma.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on aldesleukin + zidovudine + ganciclovir.