Monthly Archives: October 2020

An EGFR-MET bispecific antibody-Amivantamab(JNJ-372) combine with 3rd generation EGFR TKI-Lazertinib demonstrated safety and efficacy in a phase I trial

In an expansion cohort of a phase I CHRYSALIS study, the RP2CD (recommended phase 2 combination dose) of amivantamab antibody combined with 3rd generation EGFR TKI lazertinib to exam patients in osimertinib resistant(n=45) or treatment-naïve(n=20) EGFR-positive (exon 19 deletions and L858R) NSCLCs. In osimertinib resistant group, the objective response rate(ORR) was 36% with one patient complete response, response was seen irrespective of first or second lines used osimertinib.

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Poziotinib showed potential in treating NSCLC patients harboring an ERBB2 Exon 20 insertion

ERBB2 exon 20 insertion accounts for 2-3% of the total mutations of non-small cell lung cancer. However, there is still an unmet need for treating patients with this kind of mutation. The phase 2 ZENITH20 trial is aimed to study the activity of poziotinib in NSCLC patients with either an EGFR exon 20 insertion or an ERBB2 exon 20 insertion.

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The biomarker exploratory analyzed results of the phase 3 JAVELIN Bladder 100 trial

Urothelial carcinoma (UC) is one of the malignant diseases with a poor five-year survival rate. Platinum-based regimen is the major treatment option for patients with UC. Recently, immune checkpoint inhibitors had been demonstrated anti-tumor activity in UC. Avelumab is an anti–PD-L1 antibody that has been approved with first-line maintenance treatment in UC followed the phase 3 JAVELIN Bladder 100 trial.

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Acepodia to Present at the 7th Annual China Healthcare Summit

SAN FRANCISCO and TAIPEI, Taiwan, Oct. 22, 2020 (GLOBE NEWSWIRE) — Acepodia, a biotechnology company developing novel off-the-shelf cell therapies against solid-tumor and hematologic cancers, today announced that Sonny Hsiao, Ph.D., chief
executive officer, will present a corporate overview at the upcoming 7th Annual China Healthcare Summit on November 9, 2020.

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