TYK Medicines reports superior interim Phase II data for asandeutertinib versus osimertinib in first-line EGFR-mutant NSCLC with brain metastases

Bulletin Express05-31

TYK Medicines (02410.HK) released interim results from the pivotal Phase II ESAONA study comparing asandeutertinib (TY-9591) with osimertinib as first-line therapy for epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) patients with brain metastases. Findings were presented as a late-breaking abstract at the 2026 American Society of Clinical Oncology annual meeting.

The open-label, multicentre trial randomised 224 untreated patients 1:1 to receive asandeutertinib 160 mg once daily or osimertinib 80 mg once daily. Primary endpoints were intracranial objective response rate (iORR) and intracranial progression-free survival (iPFS) assessed by blinded independent central review (BICR).

Key intracranial efficacy data: • BICR-confirmed iORR reached 95.50 % for asandeutertinib versus 79.60 % for osimertinib, yielding a 15.62 % difference (95 % CI: 6.66 %–24.34 %; P = 0.0004). • Median BICR-iPFS was not reached in the asandeutertinib arm and 17.51 months in the comparator arm (HR = 0.46; 95 % CI: 0.28–0.76; P = 0.0020). Eighteen- and 24-month iPFS rates were 75.24 % and 61.56 % for asandeutertinib versus 48.12 % and 38.28 % for osimertinib, respectively. • Investigator-assessed analyses confirmed the intracranial advantage, with iORR of 92.80 % versus 77.90 % (P = 0.0019) and median iPFS not reached versus 17.51 months (HR = 0.56; P = 0.0122).

Systemic efficacy also favoured asandeutertinib: BICR-confirmed overall response rate was 89.20 % versus 77.90 % (P = 0.0301), and median progression-free survival was not reached versus 17.22 months (HR = 0.64; P = 0.0473). Overall survival data remain immature.

Safety profiles were manageable. Treatment-emergent adverse events (TEAEs) occurred in 100 % of asandeutertinib recipients and 99.10 % of osimertinib recipients. Grade ≥3 TEAEs were reported in 49.50 % and 21.20 % of patients, respectively, with four permanent discontinuations due to treatment-related events in each group. Most high-grade events resolved after symptomatic management or dose reduction.

The New Drug Application for asandeutertinib has been accepted by China’s Center for Drug Evaluation and granted priority review. Progression-free survival and overall survival follow-up continues, alongside additional monotherapy and combination studies in China.

Investors are reminded that successful development and commercialisation are not guaranteed, in line with Rule 18A.05 disclosure requirements.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Comments

We need your insight to fill this gap
Leave a comment