Updated on 30 August 2012
The first clinical trial will be conducted in New Zealand and the US
Singapore: The US Food and Drug Administration (FDA) has granted approval for PR610, an anticancer "stealth" drug invented in New Zealand, to move forward to human clinical trials through its approval of an investigational new drug (IND) application for the drug.
PR610 belongs to a new class of hypoxia-activated pro-drugs for the treatment of cancer, designed by Dr Jeff Smaill and Dr Adam Patterson from the Auckland Cancer Society Research Centre (ACSRC) and Maurice Wilkins Centre for Molecular Biodiscovery. It is licensed to Proacta, a San Diego-based biotechnology company that last year engaged in the collaboration for research, development, and commercialization of PR610 in Japan with Yakult Honsha. Proacta announced today that the IND had been approved, allowing this novel first-in-class treatment to enter human trials.
The first clinical trial, a phase I/II study, will be conducted at Auckland City Hospital, Waikato Hospital and sites in the US. Patient enrollment is expected to commence in the coming weeks. Initially, the trial will recruit small groups of study-eligible patients to different dose levels of PR610 followed by monitoring of its side-effects, blood levels and anti-tumour activity.
Initial development of PR610 will focus on patients with non-small cell lung cancer who have become resistant to reversible tyrosine kinase inhibitors such as erlotinib or gefitinib. Currently, there is no effective treatment when these patients relapse. The phase I part of the phase I/II trial will investigate suitable doses in patients with solid tumors, before moving on to focus on patients with this type of cancer in the phase II part of the trial.
PR610, which specifically targets low-oxygen (hypoxic) regions in tumors, has shown promising activity in the laboratory. "The tumor dose intensity achieved by this hypoxia targeting technology results in striking anti-cancer activity," says Dr Smaill. "We were particularly impressed when we compared PR610 to existing clinical candidates," adds Dr Patterson. "Only PR610 was able to shrink the drug-resistant lung cancer models."