Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This entry refers to a combination of the nucleoside analog azvudine and the antibiotic trimethoprim-sulfamethoxazole; however, clinical and pipeline data from Genuine Biotech indicate that the intended therapeutic combination for lymphoma is **azvudine plus cyclophosphamide (CTX)**. Azvudine is a small molecule DNA synthesis inhibitor and immunomodulator that terminates DNA chain elongation in malignant cells. In the lymphoma program, it is combined with cyclophosphamide, an alkylating agent that cross-links DNA, to achieve synergistic anti-tumor effects. Preclinical studies of the azvudine/cyclophosphamide combination demonstrated complete tumor elimination in lymphoma models. Trimethoprim-sulfamethoxazole is typically used as prophylaxis against opportunistic infections (such as Pneumocystis pneumonia) in immunocompromised patients but is not the primary chemotherapy agent in this regimen.
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 azvudine + trimethoprim + sulfamethoxazole.