Quantum BioPharma Partners with Thermo Fisher to Launch Phase 2 Trial of Lucid-MS, a Potential First-in-Class Myelin-Protecting Multiple Sclerosis Therapy

Quantum BioPharma has signed a Study Start-Up Agreement with Thermo Fisher's clinical research business to initiate a Phase 2 trial of Lucid-MS, a novel neuroprotective drug candidate for progressive multiple sclerosis, potentially addressing a significant unmet need.

LA Metrowire Staff
••Healthcare
Quantum BioPharma Partners with Thermo Fisher to Launch Phase 2 Trial of Lucid-MS, a Potential First-in-Class Myelin-Protecting Multiple Sclerosis Therapy

Quantum BioPharma (NASDAQ: QNTM), a biopharmaceutical company focused on neurodegenerative and metabolic disorders, has signed a Study Start-Up Agreement with the clinical research business of Thermo Fisher Scientific to implement the Phase 2 trial of Lucid-MS, its lead drug candidate for multiple sclerosis (MS). The agreement, announced by Quantum BioPharma (NASDAQ: QNTM), moves Lucid-MS from planning into execution and sets the stage for a rigorous clinical test of a treatment approach that differs from most existing MS therapies.

"Following FDA clearance to proceed with the phase 2 study, initiating study start-up activities with a leading global CRO with extensive CNS and MS experience represents an important next step," said Quantum BioPharma CEO Zeeshan Saeed. The company had previously signed the agreement, and the FDA had cleared the Investigational New Drug application for Lucid-MS in August.

The collaboration matters because MS affects an estimated 3 million people worldwide, including nearly 1 million in the United States. The disease damages myelin, the protective coating around nerve fibers, and is often disabling. Most MS drugs work by quieting the immune system, but Lucid-MS is designed around a novel neuroprotective approach that targets demyelination rather than solely modulating the immune system. "Lucid-MS is designed around a novel neuroprotective approach that targets demyelination rather than solely modulating the immune system," noted Andrzej Chruscinski, Quantum's President of Scientific and Clinical Affairs. "The phase 2 study will provide an important opportunity to evaluate the innovative approach using clinical and radiological measures."

The need is especially acute for progressive forms of MS, which are the focus of the Lucid-MS trial. A 2023 study in Neurology and Therapy described treatment options for progressive MS as limited, finding that many patients remain untreated or continue to decline despite available therapies. A National MS Society report released this year drew on survey responses from more than 2,800 people living with MS and identified urgent unmet needs, including effective treatment of disease progression and therapies that repair myelin damage.

Thermo Fisher's clinical research business, which the company acquired in 2021 for $17.4 billion, is a leading global contract research organization with deep expertise in central nervous system and MS studies. "We're proud to partner with Quantum BioPharma in advancing their neuro-degenerative clinical program in multiple sclerosis," said Michael Cioffi, vice president and general manager, neuroscience, clinical research, at Thermo Fisher. "Our team brings deep experience in CNS and MS trials, along with an integrated approach that connects strategy and execution to help deliver these complex studies."

Lucid-MS is an investigational, first-in-class new chemical entity that targets peptidyl arginine deiminase 2 (PAD2), an enzyme implicated in the hypercitrullination of myelin proteins. By inhibiting PAD2, Lucid-MS is being investigated for its potential to protect the integrity of the myelin sheath. In preclinical models, the compound has demonstrated the ability to prevent and reverse measures of myelin degradation. It has also shown a favorable safety profile and was well tolerated in Phase 1 trials in healthy participants.

The commercial stakes are notable. Quantum's announcement cites Grand View Research in projecting that the MS therapeutics market will exceed $38 billion by 2030. The randomized, double-blind, placebo-controlled Phase 2 trial will evaluate the efficacy, safety and tolerability of Lucid-MS in people with progressive MS, assessing clinical and radiological endpoints tied to disease progression. For more information, visit www.QuantumBioPharma.com. The latest news and updates relating to QNTM are available in the company's newsroom at https://ibn.fm/QNTM.

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