CHM chimeric therapeutics limited

Ann: Trading Halt, page-30

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    The safety and efficacy of Tecartus was established in a multicenter clinical trial of 60 adults with refractory or relapsed MCL who were followed for at least six months after their first objective disease response. The complete remission rate after treatment with Tecartus was 62 percent, with an objective response rate of 87 percent.

    The label carries a boxed warning for cytokine release syndrome (CRS), which is a systemic response to the activation and proliferation of CAR-T cells causing high fever and flu-like symptoms, and for neurologic toxicities. Both CRS and neurologic toxicities can be fatal or life-threatening. The most common side effects of Tecartus include serious infections, low blood cell counts and a weakened immune system. Side effects from treatment usually appear within the first one to two weeks after treatment, but some side effects may occur later.

    The above is from a erite up of the approval of another CarT. It shows how an accelerated approval trial does not need s large cohort of patients, can be completed in a reasonably quick timeframe, and not be held back by sometimes fatal adverse responses.

    This is still further down the road for CHM, but positive feedback this week leads us directly to that point.

    CarT drugs and treatments are expensive. Most costing circ $us500k for a one off treatment.
 
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