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NEW YORK DAWN™ > Blog > Health > Cell remedy for sufferers with amyotrophic lateral sclerosis exhibits promise in human trials
Cell remedy for sufferers with amyotrophic lateral sclerosis exhibits promise in human trials
Health

Cell remedy for sufferers with amyotrophic lateral sclerosis exhibits promise in human trials

Last updated: May 24, 2025 6:34 am
Editorial Board Published May 24, 2025
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Credit score: Pixabay/CC0 Public Area

Dr. Simrit Parmar, an affiliate professor within the School of Drugs at Texas A&M College and founding father of the clinical-stage biotech firm Cellenkos Inc. in Houston, has invented a brand new cell remedy that exhibits sturdy promise for the remedy of amyotrophic lateral sclerosis (ALS), aplastic anemia and different devastating illnesses.

Her remedy has been evaluated in dozens of human sufferers and has been proven to be protected and, up to now, efficient.

“If we succeed, millions of lives could be improved—organically, systematically and without significant side effects,” Parmar says.

Her outcomes are promising sufficient to draw a serious funding and partnership between Cellenkos and the main medical heart in Riyadh, Saudi Arabia. Introduced Could 22, it’s the first alliance for medical medical trials between the U.S. and Saudi Arabia.

Outcomes even have led to 2 latest articles in NEJM Proof. The articles draw consideration to promising potential remedies for sufferers with aplastic anemia and ALS.

Parmar is giving hope to sufferers with a newly developed use of umbilical twine blood-derived T regulatory (Treg) cell remedy. The remedy treats the irritation on the heart of quite a few hard-to-treat or untreatable diseases. Derived from umbilical twine blood (CB), these Tregs are naturally wired to resolve irritation with out changing into dangerous themselves.

The three key elements of Parmar’s innovation are:

The cell remedy doesn’t require matching a person donor to a person affected person.
The cell remedy might be manufactured at scale, the place a single beginning CB unit can generate a number of ready-to-use merchandise that may be frozen for as much as three years and thawed later to be used. This solves monumental logistical challenges related to different cell-based remedies.
Through the use of umbilical cord-derived cells, the remedy sidesteps the risks posed by adult-derived Tregs, which carry an elevated threat of additional irritation.

Breakthrough cell therapy for patients with ALS and other devastating diseases

Credit score: NEJM Proof (2025). DOI: 10.1056/EVIDoa2400249

Parmar is addressing situations the place typical remedies have failed. Her staff has handled greater than 80 sufferers affected by a number of situations, together with ALS, aplastic anemia, myelofibrosis and acute respiratory misery syndrome (ARDS).

In April 2025, NEJM Proof highlighted a examine of Parmar’s expertise for the remedy of ALS, the place a number of infusions led to enchancment in sufferers’ perform decline.

In Could 2024, the journal highlighted a examine of her expertise within the remedy of aplastic anemia, the place a single infusion of her remedy led to sturdy independence from sufferers’ blood and platelet transfusions for as much as 3.5 years.

The settlement between Cellenkos and King Faisal Specialist Hospital & Analysis Centre in Riyadh will start with two medical trials in Saudi Arabia for aplastic anemia and graft-versus-host illness and can pave the way in which for enlargement into research of sufferers with ALS and cardiovascular illnesses. Cellenkos can even help the Saudi Analysis Middle with coaching and training in cell and gene remedy manufacturing.

Within the U.S., Parmar hopes to have regulatory approval from the FDA in about two years for remedies of sure illnesses, together with aplastic anemia. She is also searching for funding for bigger analysis research of ALS sufferers within the U.S.

Parmar was within the lymphoma and myeloma division at MD Anderson Most cancers Middle in Houston till final fall and previous to that, within the division of stem cell transplantation. She was drawn to the Texas A&M School of Drugs as a part of a broader effort by the Texas A&M College System to strengthen well being sciences innovation amongst researchers.

“Dr. Parmar is working on absolutely transformational technology,” stated John Sharp, chancellor of the Texas A&M System. “We’re proud that she has brought her innovative skills and dedication to improving patients’ lives to the Texas A&M faculty.”

Normal (Ret.) Mark A. Welsh III, president of Texas A&M College, additionally acknowledged Parmar’s contributions.

“Texas A&M University researchers, like Dr. Parmar, are driving innovation in the most crucial areas, solving problems to build a brighter, safer world for the people of Texas, the nation and beyond,” Welsh stated. “We look forward to seeing the positive impact this invention will have, and we’re incredibly proud of Dr. Parmar and her work in this space.”

Extra info:
Neil A. Shneider et al, Medical Security and Preliminary Efficacy of Regulatory T Cells for ALS, NEJM Proof (2025). DOI: 10.1056/EVIDoa2400249

Supplied by
Texas A&M College

Quotation:
Cell remedy for sufferers with amyotrophic lateral sclerosis exhibits promise in human trials (2025, Could 23)
retrieved 24 Could 2025
from https://medicalxpress.com/information/2025-05-cell-therapy-patients-amyotrophic-lateral.html

This doc is topic to copyright. Other than any truthful dealing for the aim of personal examine or analysis, no
half could also be reproduced with out the written permission. The content material is offered for info functions solely.

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