Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
QL-1706 + modified TPF regimen is a combination therapy being investigated for the treatment of locally advanced nasopharyngeal carcinoma. QL-1706 (also known as iparomlimab/tuvonralimab or PSB205) is a first-in-class bifunctional antibody mixture developed using proprietary MabPair technology, which allows for the simultaneous production of two distinct monoclonal antibodies—iparomlimab (an anti-PD-1 IgG4 antibody) and tuvonralimab (an anti-CTLA-4 IgG1 antibody)—from a single cell line. The modified TPF regimen in this specific clinical context consists of albumin-bound paclitaxel (a microtubule stabilizer), cisplatin (a DNA-crosslinking agent), and S1 (an oral fluoropyrimidine consisting of tegafur, gimeracil, and oteracil). This combination aims to leverage the synergistic effects of dual immune checkpoint blockade and cytotoxic chemotherapy to improve outcomes in patients with nasopharyngeal carcinoma. The regimen is currently being evaluated in a Phase 2 clinical trial led by The First Affiliated Hospital of Xiamen University.
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 QL-1706 + albumin-bound paclitaxel + cisplatin + S1.