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Home » Topics » Financings » Grant

Grant
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3D illustration showing presence of tumor inside prostate gland
Cancer

Critical Path Institute funds development of QED-203 for advanced prostate cancer

May 14, 2025
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Critical Path Institute’s Translational Therapeutics Accelerator has invested in the development of QED-203 for advanced and therapy-resistant prostate cancer. Based on research at the University of Queensland’s School of Pharmacy and Pharmaceutical Sciences, QED-203 is being developed by the Queensland Emory Drug Discovery Initiative.
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Enterobacteriaceae
Infection

Arrepath’s antibiotic targeting Enterobacterales receives CARB-X funding

April 4, 2025
Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator (CARB-X) will award Arrepath Inc. $3.7 million to execute a lead optimization workplan for its first-in-class antibiotic targeting a clinically novel target for the treatment of complicated urinary tract infections caused by multidrug-resistant Enterobacterales.
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Art concept for hematologic cancer
Immuno-oncology

French grant supports Allogenica’s universal CAR T therapy for CD19-positive hematologic cancers

March 20, 2025
Allogenica SAS has been awarded a €2.5 million (US$2.7 million) grant under the French government’s France 2030 program to help advance its universal CAR T candidate, XL-001, for CD19-positive hematologic cancers.
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Multiple sclerosis
Neurology/psychiatric

Grant supports evaluation of Myrobalan’s GPR17 antagonist for progressive MS

March 14, 2025
Myrobalan Therapeutics Inc. has been awarded a grant of over $850,000 from the National Multiple Sclerosis Society to support the preclinical and translational development of MRO-002, a G-protein-coupled receptor 17 (GPR17) antagonist, for the treatment of progressive multiple sclerosis (MS).
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Colorized scanning electron micrograph of E. coli bacteria.
Immune

CARB-X funds Immunethep’s conjugated peptide-based vaccine for E. coli infections

Feb. 26, 2025
CARB-X (Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator) has announced it will award US$2 million to Immunethep SA to develop a conjugated peptide-based vaccine to prevent infections from all invasive serotypes of Escherichia coli.
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Cancer

DoD funding supports Kairos Pharma’s ENV-205

Feb. 19, 2025
Kairos Pharma Ltd. has announced that through its academic partnership with Cedars-Sinai Medical Center, Cedars-Sinai has received $600,000 in funding from the Department of Defense lung cancer research program to advance the development of ENV-205, a new drug to treat chemotherapy drug resistance and cachexia.
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Dollar sign droplet above test tube
Neurology/psychiatric

CIRM grant supports Cure Rare Disease’s antisense oligonucleotide therapy for SCA3

Feb. 7, 2025
Cure Rare Disease has been awarded a $5.69 million grant from the California Institute for Regenerative Medicine (CIRM) to advance the development of an antisense oligonucleotide therapy for spinocerebellar ataxia type 3 (SCA3).
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Neurology/psychiatric

CIRM grant supports Navega’s gene therapy for chronic pain

Feb. 5, 2025
Navega Therapeutics Inc. has received a $4 million Translational Science grant from the California Institute for Regenerative Medicine (CIRM) to support its work addressing neuropathic pain. The grant will fund the final preclinical development studies of NT-Z001 leading to an IND submission.
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Illustration of immunoglobulin A with secretory IgA
Immune

Lactiga’s secretory IgA replacement therapy for compromised immune function receives NIAID funding

Feb. 4, 2025
Lactiga Inc. has been awarded a multiyear grant by the National Institute of Allergy and Infectious Diseases (NIAID) to accelerate the advancement of the company’s lead asset, LCTG-001.
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Brain and DNA
Neurology/psychiatric

UCLA receives grant to support development of HSC gene therapy for Angelman syndrome

Jan. 31, 2025
California Institute for Regenerative Medicine (CIRM) has awarded a $5.8 million translational research grant to a scientist at the University of California, Los Angeles (UCLA) to further support the development of a hematopoietic stem cell (HSC) gene therapy to treat Angelman syndrome, including preparation of a pre-IND package submission to the FDA.
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