VAX014 is being investigated for safety, tolerability, and efficacy following intratumoral administration in patients with advanced solid tumors in a multi-center Phase 1 clinical trial. The dose escalation component of the trial is nearly complete after which an expansion phase will be initiated in combination with systemic immune checkpoint blockade.
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VAX014 has previously been investigated for the topical intravesical treatment of non-muscle invasive bladder cancer in a Phase 1 study in patients with low grade papillary (TaG1) NMIBC. This study is now closed, but demonstrated a good safety profile and antitumor activity. Future studies in NMIBC and other genitourinary cancers are part of the long term plan for VAX014.
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