Question · Q2 2026
Ed Wu inquired about the possibility of another interim data analysis for the CALMA trial, the rationale behind the recent divestment of a business unit, and plans for seeking Canadian approval for IGC 81 in parallel with FDA approval.
Answer
Ram Mukunda, CEO of IGC Pharma, stated that no further interim data analysis is expected, with the focus now on the final readout. He clarified that the company divested its non-core Vancouver manufacturing facility, not the white label business, to eliminate $600,000 in annual operating expenses, redirect resources to the CALMA trial and other assets, and secure long-term preferential supply rights for the white label business, along with a 10% contingent share of future sale proceeds for the facility. Regarding Canadian approval, Mr. Mukunda confirmed the plan is to seek approval in both the U.S. and Canada, as Health Canada has already approved the trial.
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