Japan panel approves two iPS-derived drugs in world first

Japan's health ministry panel on Thursday approved the commercialization of two regenerative medicine products derived from iPS cells, marking a global first. These treatments target patients with severe heart failure and Parkinson's disease, under a conditional approval requiring data collection for up to seven years. Shinya Yamanaka, pioneer of iPS cell research, expressed delight at this milestone.

Japan's health ministry expert panel on Thursday recommended that the minister approve the production and sale of two regenerative medical products using induced pluripotent stem (iPS) cells, poised to be the world's first of their kind.

One is ReHeart, developed by Cuorips Inc., a startup from Osaka University. It targets patients with severe heart failure due to ischemic cardiomyopathy. Heart muscle sheets derived from human iPS cells are placed on the heart's surface to promote new blood vessel formation and restore function. In 2020, an Osaka University team performed the world's first such transplant. By 2023, trials on eight patients confirmed safety and efficacy, showing reduced symptoms like exhaustion and palpitations, plus improved heart function and physical fitness.

The other is Amchepry, from Sumitomo Pharma Co. and Racthera Inc., for Parkinson's disease. iPS cells are differentiated into dopaminergic neural progenitor cells and injected into the brain. Trials from 2018 to 2023 at Kyoto University Hospital and others involved seven patients in their 50s and 60s; six were assessed. The cells produced dopamine, and four showed motor function improvements after two years of observation. No serious side effects occurred, with better results in younger patients with milder symptoms.

iPS cells were pioneered by Shinya Yamanaka, who generated mouse iPS cells in 2006 and human ones in 2007, earning the 2012 Nobel Prize in Physiology or Medicine. Using patient-derived cells aims to minimize rejection, though long-term safety remains a challenge. The approvals are conditional based on small trials, with rollout pending discussions on pricing, insurance, and manufacturing. Cuorips aims to launch sales this year.

Yamanaka said, "I am very happy to see the first big step toward its societal implementation, 20 years since it was announced." The panel set a seven-year approval term; if safety is later confirmed, full use without restrictions will be allowed.

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Scientists in a lab celebrating conditional approval of iPS cell products for treating Parkinson's and heart disease.
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Health ministry panel conditionally approves iPS cell products

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A health ministry expert panel has conditionally approved two regenerative medicine products derived from induced pluripotent stem (iPS) cells for treating Parkinson's disease and severe heart disease. This marks a potential world first in commercializing Nobel Prize-winning stem cell technology. The approval, based on small-scale clinical trials confirming safety and presumed efficacy, requires post-market verification within seven years.

Doctors at Keck Medicine of USC are implanting lab-grown, dopamine-producing cells into the brains of people with Parkinson’s disease in an early-stage clinical trial that will enroll up to 12 participants across three U.S. sites.

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Keck Medicine of USC researchers are testing an experimental approach to Parkinson’s disease that implants lab-grown, dopamine-producing cells into a movement-control region of the brain. The early-stage Phase 1 REPLACE trial involves up to 12 people with moderate to moderate-severe Parkinson’s disease, and the U.S. Food and Drug Administration has granted the study fast-track designation.

A Cold Spring Harbor Laboratory study demonstrated CAR T-cell therapy can reverse age-related intestinal decline in mice by targeting senescent cells. While promising, experts caution on safety risks, off-target effects, dosing, and costs for human use.

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Cold Spring Harbor Laboratory researchers report that engineered anti-uPAR CAR T cells cleared senescence-linked cells in mice, improving intestinal regeneration, reducing inflammation and strengthening gut barrier function. The approach also aided recovery from radiation-related intestinal injury and showed regenerative signals in experiments using human intestinal and colorectal cells, raising the possibility of future clinical trials.

Duke-NUS Medical School researchers, working with the University of Sydney, have developed BrainSTEM—a two-tier, single-cell atlas of the developing human brain that profiles nearly 680,000 cells. Published online in Science Advances on October 31, 2025, the resource focuses on midbrain dopaminergic neurons, flags off‑target cell types in lab-grown models, and will be released openly for the research community.

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Japan's education ministry has certified the Institute of Science Tokyo as the second university eligible for aid from a ¥10 trillion government fund. Formed in 2024 by merging the Tokyo Institute of Technology and Tokyo Medical and Dental University, it expects over ¥10 billion in subsidies in its first year. The certification supports a plan to enhance cooperation between medical and engineering researchers.

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