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Biotech Funding

All articles tagged with #biotech funding

Caribou Biosciences closes after failing to fund pivotal CAR-T trial
biotechnology2 days ago

Caribou Biosciences closes after failing to fund pivotal CAR-T trial

Caribou Biosciences is shutting down operations and laying off staff after failing to secure funding for a Phase 3 trial of its allogeneic CAR-T therapy, vispa-cel. The company, which spun out of Nobel laureate Jennifer Doudna’s lab, had $113.8 million in cash but could not raise the capital needed to advance its pipeline. While its therapy showed efficacy comparable to approved autologous treatments, the company is seeking strategic alternatives like a sale or merger as investor interest shifts toward in vivo gene editing approaches.

Khartis targets oral IGF-1R TED pill after $95M fundraising
business1 month ago

Khartis targets oral IGF-1R TED pill after $95M fundraising

Khartis Therapeutics, led by former XinThera executives after Gilead’s acquisition, emerged with a $50M Series B (total funding now $95M) to push an oral IGF-1R inhibitor for thyroid eye disease into clinical trials in Q1 2027, aiming to replace IV therapies like Tepezza and Lumvoa; the company also has other internal programs and strong investor backing.

MeiraGTx lands up to $400M to accelerate commercialization of late-stage gene therapies
biotech3 months ago

MeiraGTx lands up to $400M to accelerate commercialization of late-stage gene therapies

MeiraGTx secured up to $400 million from Oberland Capital to push its late-stage gene therapies toward launch, anchored by an initial $125 million loan with low single-digit royalties and a $10 million equity stake. The deal also includes up to $50 million in milestones for FDA approvals (one per program for bota-vec and AAV2-hAQP1), up to $100 million more via mutual commitments, and a right for Oberland to buy an additional $15 million in equity. In addition, $50 million could follow a positive AQUAx2 phase 2 readout for dry mouth. Beyond bota-vec and AAV2-hAQP1, MeiraGTx is advancing AAV-GAD for Parkinson’s, with a 2029 follow-up study, and noted a 2025 Lilly license for AAV-AIPL1, highlighting a pipeline with several near-term regulatory milestones.