FDA - RNS25 Jun 2024 10:04
New cancer treatment with the potential to slow brain tumor growth is now available to patients in the US with relapsed/refractory histologic or molecular glioblastoma
Imaging Biometrics, LLC ("IB"), the Wisconsin USA based subsidiary of IQ-AI (LSE: IQAI), announces that the US Food and Drug Administration ("FDA") has approved an Expanded Access Program ("EAP") for oral gallium maltolate ("GaM").
This EAP will run in parallel with the current phase 1 clinical trial being conducted at the Medical College of Wisconsin ("MCW"). As the phase 1 trial concludes this fall and while the data is being compiled, eligible patients in the US will have the option of participating in the EAP. Several patients have registered to participate in the EAP, and a total of 40 patients can enrol in this initial phase.
"Providing eligible patients access to GaM as a potential treatment ahead of regulatory approval underscores our commitment to helping address a clear unmet patient need," said Trevor Brown, CEO of IQAI.