Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Afatinib + ritonavir** is a combination of two pharmaceutical drugs: afatinib, an irreversible oral ErbB family (EGFR, HER2, HER4) tyrosine kinase inhibitor primarily indicated for non-small cell lung cancer, and ritonavir, a protease inhibitor used predominantly as a pharmacokinetic enhancer due to its potent inhibition of CYP3A and P-glycoprotein (P-gp). Ritonavir increases systemic exposure to drugs that are substrates of these pathways, especially by inhibiting P-gp activity, which reduces drug efflux and increases absorption of co-administered agents like afatinib. This combination does not have a unique brand or code name and is not established as a marketed or investigational product, but both drugs are occasionally coadministered with attention to pharmacokinetic interactions. The combination may mildly increase afatinib exposure, depending on the timing of administration, but this can be managed by separating doses or adjusting afatinib dosage, and clinical interaction is not viewed as highly significant if managed appropriately[1][2][3][4][5].
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 afatinib + ritonavir.