Highlights
- HREC approval enables conducting a Phase 1 therapeutic study in patients with PDL1-positive NSCLC.
- GenesisCare Contract Research Organization would support the study.
- NSCLC is the most common type of lung cancer.
Radiopharm Theranostics Limited (ASX: RAD) has received Human Research Ethics Committee (HREC) approval to undertake a Phase 1 therapeutic study in patients with PDL1- positive non-small cell lung cancer (NSCLC). This is the company’s first-in-human Phase 1 study in Australia for its therapy in this condition.
The dose escalation trial of RAD204 aims to assess the efficacy and safety of this radiotherapeutic in patients with PDL1-positive NSCLC.
The study would take place at Alexandra Hospital in Brisbane, Australia, with the assistance of GenesisCare, an oncology care provider.
Data source: Company update
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Triggered by the update, RAD’s share price increased by 3.85% to trade at AU$0.14 apiece at the time of writing on 9 October 2023.
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RAD’s proprietary nanobody from the NanoMab platform is the technology which underpins the Phase 1 therapeutic study, targeting PDL1-positive NSCLC, the most common type of lung cancer.
The company highlighted that in Australia, around 12,200 patients are diagnosed with lung cancer annually, making it the fifth most common cancer in the nation. Globally, in 2020, over 2.2 million lung cancer cases were reported, out of which NSCLC accounted for ~85% of the cases.
This is an area of high unmet need and there is potential for the treatment to be the “first in class” radiopharmaceutical therapy targeting PDL1, indicates the company.
To know about RAD’s annual performance in 2023, click here.