Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**elexacaftor + tezacaftor + VX-561** is an investigational fixed-dose **triple combination therapy** developed for the treatment of cystic fibrosis. Elexacaftor and tezacaftor are CFTR (cystic fibrosis transmembrane conductance regulator) correctors that facilitate increased quantity of functioning CFTR protein at the cell surface, while VX-561 (deutivacaftor) is a deuterated form of ivacaftor that acts as a CFTR potentiator, enhancing the protein’s ability to function as a chloride channel. This once-daily combination is being evaluated in late-stage clinical trials for efficacy and safety in patients with cystic fibrosis, particularly aiming to improve upon current therapies (like Trikafta) in terms of efficacy and dosing convenience[1][2][6].
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 elexacaftor + tezacaftor + VX-561.