Jubilant Therapeutics' JBI-778 IND application receives US FDA approval to treat solid tumours with brain metastases and primary brain tumours.
M2 EQUITYBITES-August 4, 2022-Jubilant Therapeutics' JBI-778 IND application receives US FDA approval to treat solid tumours with brain metastases and primary brain tumours
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Jubilant Therapeutics Inc., a US-based biopharmaceutical company, announced on Wednesday that it has received approval from United States Food and Drug Administration (US FDA) for the Investigational New Drug application (IND) for JBI-778, an oral, brain penetrant and selective protein arginine methyl transferase 5 (PRMT5) inhibitor, intended to treat solid tumours with brain metastases and primary brain tumours including high-grade glioma.
The Phase I/II trial is an open-label, two-part dose escalation and expansion study, aimed at defining the product's safety profile, pharmacokinetics, optimal dosing and preliminary activity. The participants in the dose...
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