Therefore, a UG3/UH3 award will support the planning phase (UG3) and the implementation phase (UH3) of a single trial that has met the scientific milestones and feasibility requirements for transition. Applications designed to test the efficacy of a behavioral intervention will not be supportedby this FOA. Scope of the UG3/UH3 FOA

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Due dates: June 19, 2023 (UG3/UH3); June 20, 2023 (U44); Both: October 18, 2023; February 20, 2024, June 20, 2024 Award Budget: Application budgets are not limited but need to reflect the actual needs of the proposed project and should only cover the work that will be performed by the PD/PI and their staff.

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The UG3 phase will permit both scientific and operational planning activities. The UH3 phase of the award will support the clinical trial of the drug, biologic, device, or behavior intervention (and if needed, additional scientific studies). The UG3 Phase may not exceed 2years. The UH3 Phase may not exceed 4 years.

Phased cooperative agreement mechanisms (UG3/UH3 and SBIR U44 Fast-Track) support pre-clinical/translational device activities, including translational …

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The UG3/UH3 application must be submitted as a single application with the design of a sample UH3 clinical trial described in the application, following the instructions described in this FOA. The UG3 phase permits preclinical, translational, and IND-enabling studies. The UH3 phase must include initiation and conduct of an early phase, proof-of ...

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The core milestones must be met during the UG3 phase to allow for successful launch of the full trial in the UH3 phase of the clinical trial. The overall planned enrollment and percentage of active clinical sites expected by the end of the UG3 phase will be agreed upon between the grantee organization (or recipient) and the NHLBI prior to …

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Frequently Asked Questions for DECIPHeR UG3/UH3 (RFA-HL-20-003) Q1. When are applications due? A1. A change in the application receipt dates for the two …

52 rowsUG3/UH3. Expiration Date. 01/08/2027. NIDCR supports well-designed clinical trials (Phase I, II, III, and IV) that have the potential to improve oral and craniofacial health.

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At the first meeting in the UG3 phase of the collaborative CCC, the DSMB will review the awardee's protocol and potentially recommend modifications. Subsequently, …

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Funding period: The grant mechanism used to support this funding announcement is a cooperative agreement (UG3/UH3) mechanism with two phases. …

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The upcoming application due dates for PAR-20-122 (UG3/UH3) and PAR-20-111 (U44) are: August 9, 2022; February 9, 2023; August 9, 2023.

UG3/UH3 phase transition and Milestones. This funding opportunity is designed as a two-stage cooperative agreement in which Project Scientists from NIAID will work with the investigative team. It will support projects that are organized into a two-year UG3 phase followed by a three-year UH3 phase. The UG3 phase may include pilot, …

The UG3/UH3 milestone-driven NCI-collaborative grant mechanism will allow recipients to explore novel cell therapy approaches and to generate preclinical IND-enabling data during the initial UG3 phase, and then rapidly test these approaches in early phase, proof of concept, or first-in-human clinical trials in the UH3 phase.

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R01 Guidelines. R03. Small Research Grants. Active R03 funding opportunity: PAR-22-119. The Limited Competition: Small Grant Program for NIAMS …

UG3/UH3 Cooperative Agreement Award Mechanism This FOA will utilize a two-phase cooperative agreement (UG3/UH3) mechanism. Awards made under this …

The UG3/UH3 is a phased cooperative agreement award. The BPN uses the UG3/UH3 award to pay for work that will be conducted by the Principal Investigator (PI). The UG3 supports the PI's activities during the preparatory phase, while the UH3 supports subsequent work. BPN applicants can request up to one year of UG3 support.

HEAL Initiative: Non-addictive Analgesic Therapeutics Development [Small Molecules and Biologics] to Treat Pain (UG3/UH3 Clinical Trial Optional) Reissue of RFA-NS-20-010: The purpose of this funding opportunity announcement (FOA) is to support preclinical optimization and development of safe, effective, and non-addictive small molecule and ...

The Rochester-Magee award in the first phase of ECHO (UG3/UH3 OD023349) was a pregnancy cohort that followed children through age 4 years. In this proposal, which is responsive to RFA-OD-22-018 for the second phase of ECHO, we will recruit an additional pregnancy cohort of 375 pregnancies (across the first 5 years) and conduct a pediatric ...

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