BerGenBio Announces Safety Data from Dose Escalation Phase 1b in First Line NSCLC Patients
Ph1b data support safety, predictable PK and adequate plasma exposure
The Phase 1b part of the study evaluated three escalating doses of
Key conclusions include:
- All three selected doses demonstrated that the triplet combination is well tolerated with no new safety signals identified, supporting the further clinical development of bemcentinib and CIT in 1L NSCLC patients.
- No dose-related impact on electrocardiographic changes (QTc), a known class effect of tyrosine kinase inhibitors, was reported for bemcentinib during the observation period.
- Pharmacokinetic analyses confirmed adequate plasma exposure of bemcentinib, achieving levels consistent with that previously observed in responders in
BerGenBio's BGBC008 study of bemcentinib and pembrolizumab in second-line NSCLC patients.
Contacts
ir@bergenbio.com
rune.skeie@bergenbio.com
Investor Relations / Media Relations
jl@lillebyfrisch.no
About STK11m NSCLC
Patients with STK11m NSCLC have a significantly poorer response to current therapies, including immune checkpoint inhibitors, when compared with patients with wild-type (non-mutated) STK11. AXL plays a significant role in the survival and spread of cancer and STK11m NSCLC patients have a high expression of AXL suggesting that AXL is an important target to prevent disease progression and resistance to existing therapies. Bemcentinib's selective inhibition of AXL has been shown to improve the response to immune checkpoint inhibition in STK11m patient-derived preclinical models and in early clinical studies. There are currently no targeted therapies available for the STK11m NSCLC patient population, which represents up to 20% of 1L NSCLC patients.
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