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Tiziana Life Sciences Announces Groundbreaking ALS Trial Grant Awarded by the ALS Association

TLSA 11.19.2024

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Drug:anti-CD3-monoclonal-antibody intranasal foralumab

Diseases:Amyotrophic Lateral Sclerosis (ALS)

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NEW YORK,Nov. 19, 2024(GLOBE NEWSWIRE) --Tiziana Life Sciences, Ltd.(Nasdaq: TLSA) (“Tiziana” or the “Company”), a biotechnology company developing breakthrough immunomodulation therapies with its lead development candidate, intranasal foralumab, a fully human, anti-CD3 monoclonal antibody, today announced that its grant application to theALS Associationhas been approved for funding. The grant is awarded as part of the Hoffman ALS Clinical Trial Awards Program and is titled “Modulation of ALS neuroinflammation by nasal anti-CD3 monoclonal Antibody”. The Association’s grant will fund a 20-patient clinical trial of two doses of Tiziana’s novel and patented therapeutic candidate, intranasal foralumab, aimed at evaluating the safety and early-stage parameters of disease improvement in Amyotrophic Lateral Sclerosis (ALS), also known asLou Gehrig'sdisease.

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord, ultimately leading to muscle weakness and paralysis. ALS is an orphan disease, but its clinical course can be rapid with marked disability even at an early stage. Over the course of the disease, people lose the ability to move, to speak, and eventually, to breathe. The disease is always fatal, usually within five years of diagnosis. Few treatment options exist, resulting in a high unmet need for new therapies to address functional deficits and disease progression.

“The Hoffman ALS Clinical Trial Awards Program supports early-stage clinical trials of potential new therapies that hold promise for those living with ALS,” saidKuldip Dave, Ph.D., Senior Vice President of Research at theALS Association. “With this award, we are pleased to help advance the development of intranasal foralumab for ALS. By funding programs at this early stage, we hope to accelerate the development of therapeutic candidates that can help make ALS a livable disease.”

James Berry, MD, MPH, andSuma Babu, MBBS, MS, the Director and Co-Director of theNeurological Clinical Research Institute(NCRI) atMass General Hospital, a founding member ofMass General Brigham, commented: “We are incredibly grateful to theALS Associationfor recognizing the promise of intranasal foralumab, and we are excited to initiate clinical development in ALS in hopes of identifying a novel therapy for ALS and other neurodegenerative diseases. We will be using PET imaging to detect neuro inflammation in this study of patients with ALS. We hope to replicate the previous positive findings of the PET imaging approach that Tiziana has seen in studies of patients with multiple sclerosis, in this new potential indication for intranasal foralumab.”

"We are honoured to receive this prestigious grant from theALS Association, which underscores the promising potential of our therapeutic platform in addressing the urgent needs of ALS patients. This funding will accelerate our clinical development efforts and bring us closer to potentially transformative treatment options for ALS,” saidIvor Elrifi, CEO ofTiziana Life Sciences. "Tiziana Life Sciences’ innovative approach targets the underlying mechanisms of ALS with the aim of halting or slowing disease progression. The company’s commitment to rigorous scientific research and patient-centric innovation aligns with the ALS Association’s mission to discover treatments and a cure for ALS, as well as to serve, advocate for, and empower people affected by ALS.”

The Hoffman ALS Clinical Trial Awards Program, named in honor of the late philanthropistHugh Hoffman, helps develop new and improved ALS therapies by supporting early-stage clinical trials. These trials produce data on safety, dosing, and biomarkers that are essential for advancing an investigational therapy one step closer to being evaluated by the FDA. Positive results at this stage also “de-risk” the next stage of drug development, typically large clinical trials, and help attract the follow-on funding necessary to complete this work.

Foralumab, a fully human anti-CD3 monoclonal antibody, is a biological drug candidate that has been shown to stimulate T regulatory cells when dosed intranasally. At present, 10 patients with Non-Active Secondary Progressive Multiple Sclerosis (na-SPMS) have been dosed in an open-label intermediate sized Expanded Access (EA) Program with either an improvement or stability of disease seen within 6 months in all patients. The FDA has recently allowed an additional 20 patients to be enrolled in this EA program. In addition, intranasal foralumab is currently being studied in a Phase 2a, randomized, double-blind, placebo-controlled, multicenter, dose-ranging trial in patients with non-active secondary progressive multiple sclerosis (NCT06292923).

About theALS Association

The ALS Associationis the largest philanthropic funder of ALS research in the world. The Association funds global research collaborations, assists people with ALS and their families through its nationwide network of care and certified clinical care centers, and advocates for better public policies for people with ALS.The ALS Associationis working to make ALS a liveable disease while urgently searching for new treatments and a cure. For more information about theALS Association, visit our website atwww.als.org

About theMassachusetts General Hospital

Massachusetts General Hospital, founded in 1811, is the original and largest teaching hospital ofHarvard Medical School.The Mass General Research Instituteconducts the largest hospital-based research program in the nation, with annual research operations of more than$1 billionand comprises more than 9,500 researchers working across more than 30 institutes, centers and departments. InJuly 2022, Mass General was named #8 in theU.S. News & World Reportlist of “America’s Best Hospitals.” MGH is a founding member of theMass General Brighamhealthcare system.

About Foralumab

Activated T cells play an important role in the inflammatory process. Foralumab, the only fully human anti-CD3 monoclonal antibody (mAb), binds to the T cell receptor and dampens inflammation by modulating T cell function, thereby suppressing effector features in multiple immune cell subsets. This effect has been demonstrated in patients with COVID and with multiple sclerosis, as well as in healthy normal subjects. The non-active SPMS intranasal foralumab Phase 2 trial (NCT06292923) began screening patients in November of 2023. Immunomodulation by nasal anti-CD3 mAb represents a novel avenue for treatment of neuroinflammatory and neurodegenerative human diseases.^[¹^],[²^]

AboutTiziana Life Sciences

Tiziana Life Sciencesis a clinical-stage biopharmaceutical company developing breakthrough therapies using transformational drug delivery technologies to enable alternative routes of immunotherapy. Tiziana’s innovative nasal approach has the potential to provide an improvement in efficacy as well as safety and tolerability compared to intravenous (IV) delivery. Tiziana’s lead candidate, intranasal foralumab, which is the only fully human anti-CD3 mAb, has demonstrated a favorable safety profile and clinical response in patients in studies to date. Tiziana’s technology for alternative routes of immunotherapy has been patented with several applications pending and is expected to allow for broad pipeline applications.

For more information aboutTiziana Life Sciencesand its innovative pipeline of therapies, please visitwww.tizianalifesciences.com

For further inquiries:

Tiziana Life Sciences LtdPaul Spencer, Business Development and Investor Relations+44 (0) 207 495 2379email:info@tizianalifesciences.com

[1]https://www.pnas.org/doi/10.1073/pnas.2220272120

[2]https://www.pnas.org/doi/10.1073/pnas.2309221120

Source: Tiziana Life Sciences Ltd.

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