Candel appoints Martine Zimmermann to its board of directors
Zimmermann joins with over three decades of global regulatory affairs and quality experience spanning various drug development stages.
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Clinical-stage biotech developing viral immunotherapy platforms for solid tumors
candeltx.comLast updated
In short: Candel initiated a global Phase 3 NSCLC trial, reported survival data, and advanced its prostate cancer BLA toward a Q4 2026 submission.
Zimmermann joins with over three decades of global regulatory affairs and quality experience spanning various drug development stages.
Median overall survival reached 24.5 months in advanced non-small cell lung cancer patients failing immune checkpoint inhibitors, supporting the pivotal phase 3 AURORA trial.
Aglatimagene reduces recurrence risk by 41% and induces systemic immune activation, supporting a Q4 2026 FDA application.
The company reports that phase 3 trials demonstrated meaningful improvements in disease-free survival for patients receiving the viral therapy alongside radiotherapy.
Candel Therapeutics Announces ... to ICI, Candel Therapeutics, 01 October 2026 · Aggarwal C, Sterman D, Dwyer J, Alesi ER, Maldonado F, Mehra R, et...
The announcement was made in a news release from the clinical stage biopharmaceutical company Candel Therapeutics in a final survival data report from a phase...
BofA upgrades Candel Therapeutics to Buy, citing CAN-2409 prostate cancer gene therapy and 2027...
Candel Therapeutics (CADL) upgraded from Neutral to Buy at BofA Securities; PT USD 18.00 (prev.
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