Mediar Therapeutics Secures $76M to Accelerate Anti-Fibrosis Therapies for Skin, Lung, and Kidney Diseases
A $76 million funding surge for Mediar Therapeutics signals a bold bid to reframe how aging and chronic disease are foughtāby targeting the scarring that silently undermines organs.
Mediar Therapeutics recently closed an oversubscribed $76 million Series B funding round co-led by Amplitude Ventures and ICG, with participation from Longwood Fund, Asahi Kasei Pharma Ventures, and Alexandria Real Estate Equities.
The funding will advance anti-fibrotic therapies targeting fibrotic diseases in the skin, lung, and kidney.
MTX-474, the companyās systemic sclerosis candidate, is currently in Phase 2a trials with approximately 90 patients enrolled in the EncompaSSc study. Meanwhile, MTX-463, an idiopathic pulmonary fibrosis candidate, is being developed through a $99 million upfront collaboration with Eli Lilly.
The third therapy, MTX-439 for kidney fibrosis, is scheduled to enter Phase 1 studies in 2026.
Rahul Ballal, CEO of Mediar Therapeutics, said:
"With $175 million raised through these transactions, we can advance our novel anti-fibrotics through clinical studies and potentially bring life-changing therapies to patients suffering from fibrosing diseases of the skin, lung and kidney."
Dr. Lorinda Chung, who is overseeing the Phase 2a trial for MTX-474, said:
"Patients with SSc face a large unmet need, and this Phase 2a trial will allow us to see if MTX-474 can make a meaningful difference in their lives."
Dr. Allan Marchington of ICG commented:
"Mediarās approach to the underlying causes of fibrosis is setting the stage for major clinical breakthroughs."
Dr. Bharat Srinivasa of Amplitude Ventures added:
"The organization intends to apply its scientific knowledge to develop life-changing patient therapies."
The therapies focus on inhibiting myofibroblasts, which play a central role in fibrotic disease progression. While early-stage results are promising, these findings remain preliminary and require further validation in larger clinical trials before potential clinical application.
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