SBIR/STTR Research Award

XT-101: A Potent IL-10 Based Therapy for Treating Multiple Sclerosis.

Award identifier e37651202f3d46ea3448d10000d034789474f72daa2e0c9e50457bf492e1ca44Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$689,217

Program and phase

SBIR · Phase I

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
XALUD THERAPEUTICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
LVJKCZJKEKV3
Solicitation number
PA12-088
Topic code
NINDS

Research abstract

DESCRIPTION (provided by applicant): Xalud Therapeutics proposes to evaluate the applicability of its novel and potent anti-inflammatory therapy, XT-101, for the treatment of motor impairment, gait disorders, and neuropathic pain in degenerative and inflammatory autoimmune rodent models of multiple sclerosis (MS). XT-101 is a non-viral form of gene therapy that causes the meningeal cells surrounding the spinal cord to secrete the powerful, natural, anti- inflammatory interleukin-10 (IL-10). Based on extensive pre-clinical research, Xalud believes that the secreted IL-10 will reduce inflammation and normalize the pathological microglia and astrocyte activity that is seen in MS. Xalud proposes to study XT-101 in both inflammatory and neurodegenerative rodentmodels of MS and to conduct various cell and tissue analyses to better understand and elucidate the biological effects of XT-101. Xalud expects to demonstrate in these models that XT-101 reduces motor impairment, alleviates gait disorders and resolves neuropathic pain. Xalud also expects that XT-101 will have a positive effect on numerous elements of MS pathology including: immune cell infiltration, inflammation, reduced glutamate transport, demyelination, and neuronal apoptosis. Support of the proposed studies would greatly accelerate the development of XT-101 for clinical applications. Xalud is currently conducting IND-enabling toxicology studies for the use of XT-101 in neuropathic pain and expects to file an IND in late 2013. The additional efficacy dataprovided by the proposed studies would support the initiation of human trials of XT-101 in neuropathic pain, gait disorders and possibly other MS-related indications. Xalud believes that XT-101, if successfully developed, could have a tremendous impact onthe clinical treatment of MS and greatly improve the quality of life MS patients. Neuropathic pain and gait disorders impact almost all MS patients and greatly reduce their ability to participate in society and enjoy life. Further, XT-101 may slow diseaseprogression in the currently untreatable progressive forms of MS. Because the method of action of XT-101 is markedly different from all existing or imminent MS treatments, it has the potential to be an extremely useful addition and complement to current medical practice. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Xalud Therapeutics, Inc. is seeking support to advance the development of XT-101 for the treatment of motor impairment, gait disorders and neuropathic pain associated with multiple sclerosis (MS). Currently, there are no treatments approved for MS-related neuropathic pain or for treating progressive forms of the disease and only one treatment approved for gait disorders. By addressing these areas of tremendous unmet clinical need,Xalud believes XT-101 can greatly improve the quality of life of MS patients.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

3 SBIR/STTR records share this UEI (2011–2013). Reported award amounts total $3,153,075. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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