Calico Life Sciences LLC today announced that the first participant has been dosed in a Phase 1b clinical trial, (study M23-523; NCT05757141), evaluating the investigational eIF2B activator ABBV-CLS-7262 as a potential treatment for Vanishing White Matter (VWM) disease.
| SOUTH SAN FRANCISCO, Calif., April 26, 2023 /PRNewswire/ -- Calico Life Sciences LLC (Calico), a biotechnology organization focused on the biology of aging and healthspan, and founded by Alphabet and Arthur D. Levinson Ph.D., today announced that the first participant has been dosed in a Phase 1b clinical trial, (study M23-523; NCT05757141), evaluating the investigational eIF2B activator ABBV-CLS-7262 as a potential treatment for Vanishing White Matter (VWM) disease. ABBV-CLS-7262 is being developed by Calico in collaboration with AbbVie.
VWM disease is an ultra-rare progressive leukoencephalopathy – a disease of the brain’s white matter – caused by variations in any of the five subunits of an essential enzyme in cells called eIF2B. VWM variations in eIF2B cause a reduction in its enzymatic activity that may lead to chronic activation of the integrated stress response (ISR). The ISR plays a critical role in protein homeostasis and organismal resilience, both of which are implicated in the biology of aging. When chronically activated in the brain, the ISR causes the white matter to degenerate. Individuals with VWM disease commonly have symptoms such as impaired muscle movement, cognitive decline, and seizures. While symptoms often begin to appear between ages 2 and 6, the disease can present at any age. The disease course is chronic and progressive, and stressors such as fever, infection, and mild head trauma may cause episodes of rapid deterioration. There is currently no cure and no treatment approved for VWM disease. “Since our founding, Calico has been focused on generating new scientific insights on biology relevant to aging and translating those insights to develop drug candidates for potential patient benefit,” said Arthur D. Levinson, Ph.D., founder and CEO. “ABBV-CLS-7262 is an encouraging outcome of this approach and we are pleased to advance this clinical study in vanishing white matter disease. We are grateful to all the participants in this important trial and are hopeful that ABBV-CLS-7262 will demonstrate its potential as a treatment for this devastating condition.” “We are delighted with the dedication shown by the vanishing white matter community to help start the testing of this potential treatment,” said Josh Bonkowsky, M.D., Ph.D., Professor of Pediatrics at the University of Utah and Primary Children’s Hospital. “It is exciting to be advancing this work, and it reflects major investments of time and commitment from around the world, including scientists and physicians, who have made this moment possible.” “At the Amsterdam Leukodystrophy Center we have worked long and hard to better understand vanishing white matter and help develop treatments. It is extremely meaningful and gratifying to collaborate with Calico on the clinical development of ABBV-CLS-7262,” said Marjo van der Knaap, M.D., Ph.D., Amsterdam Leukodystrophy Center, Emma Children’s Hospital and Amsterdam University Medical Center, on behalf of the International VWM Consortium of Clinical Experts. “ABBV-CLS-7262 targets the central cause of vanishing white matter and if it proves to benefit patients, would be a milestone in vanishing white matter therapy development for this disease.” This Phase 1b trial is a 96-week open-label, single arm study designed to evaluate the safety, tolerability, and pharmacokinetics of ABBV-CLS-7262 in participants diagnosed with VWM disease. This will be the first time an eIF2B activator has been administered to people with VWM disease. The study’s primary outcome measures are the assessment of adverse events over the first 7 weeks together with drug concentrations in plasma over the first 4 weeks of dosing. For more information on study NCT05757141, please visit: www.clinicaltrials.gov. About ABBV-CLS-7262 Persistent activation of the ISR has been linked to the development of several neurological disorders, and preclinical studies investigating ABBV-CLS-7262 as a modulator of the ISR have demonstrated its potential as a new therapeutic strategy. ABBV-CLS-7262 is also being investigated as a potential treatment for people with amyotrophic lateral sclerosis (ALS) in two ongoing studies; a Phase 1b study (NCT04948645), and as a regimen in the Phase 2/3 Healey ALS Platform Trial (NCT05740813), sponsored by Professor Merit Cudkowicz, M.D., M.Sc., director of the Sean M. Healey & AMG Center for ALS, chief of the Department of Neurology at Massachusetts General Hospital. ABBV-CLS-7262 is licensed from the University of California, San Francisco, based on novel technology from the lab of Peter Walter, Ph.D., Professor Emeritus of Biochemistry and Biophysics at University of California, San Francisco. ABBV-CLS-7262 is an investigational drug not yet approved for use in any country. About Calico Media Contact
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