Glioblastoma Therapeutics Network (GTN; U19 Clinical Trial Required)
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
AI Contract Overview
The National Cancer Institute (NCI) is seeking applications for research focused on developing novel therapies for adult glioblastoma (GBM) through a Notice of Funding Opportunity (NOFO). The primary objective is to improve GBM treatment by creating effective therapeutic agents capable of crossing the blood-brain barrier and advancing these agents through early-stage clinical testing. The initiative encourages the establishment of a highly collaborative Glioblastoma Therapeutics Network (GTN) consisting of interdisciplinary teams that can manage the drug development process from late preclinical stages and IND studies through to pilot clinical trials in humans. This approach aims to bridge a critical gap in GBM drug development, facilitating seamless transitions from early trials to later-stage clinical evaluations using established NCI mechanisms. Eligible therapeutic agents include completely new drugs or repurposed agents and combinations previously approved for other medical uses, provided they undergo appropriate preclinical validation for GBM. The scope of the program covers the critical transition from preclinical through Phase 0/1 clinical studies, emphasizing collaboration and integration within the network. This funding opportunity falls under the Department of Health and Human Services via the National Institutes of Health, with contact support provided by Dr. Suzanne Forry for inquiries. The program aims to accelerate the development of promising GBM treatments by leveraging multi-disciplinary teams and streamlined trial processes to bring effective therapies closer to clinical application.
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Through this Notice of Funding Opportunity (NOFO), the National Cancer Institute (NCI) solicits applications for research on novel therapies for adult glioblastoma (GBM). The goal is to improve the treatment of adult GBM by developing novel effective agents that can cross the blood brain barrier (BBB) and testing them clinically. Successful early-stage trials of new drugs from this NOFO would transition seamlessly to later stage trials using well-established NCI clinical trial mechanisms.
To implement this concept, a highly collaborative GBM Therapeutics Network (GTN) of cross-cutting teams will be established, each team capable of driving therapeutic agent(s) from pre-clinical development, through IND studies, into pilot clinical studies in humans. Appropriate therapeutic agents include: (1) novel agents or (2) agents or combinations approved for other indications and repurposed for treatment of GBM following appropriate preclinical studies. The scope of the NOFO, from late pre-clinical through early (Phase 0/1) clinical studies, uniquely spans a gap in the GBM drug development process.
