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SBIR/STTR Omnibus Webinar Recording, Transcript, and Slides Available
June 10, 2019
The Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) Program recently hosted a webinar to assist interested applicants with understanding proposal preparation, federal guidelines and resources, the funding process, and address general concerns.
The webinar presentation, recording, and transcript are now available (via web and attachments) for your reference. (Please be advised, an automated transcription service was used, and there may be grammatical errors and typos in the transcript.) We have done our best to correct as many errors as possible, but you are encouraged to reach out to us by email at sbir@od.nih.gov if anything remains unclear.
– Webinar Slides
– Recording
– Transcript
HHS SBIR and STTR Omnibus grant solicitations permit researcher-initiated topics around health, medicine and life science to be submitted for funding consideration. With any specific idea, you should speak directly with a HHS SBIR/STTR program manager at least a month BEFORE the deadline to gauge their interest.
You can find the HHS SBIR/STTR Omnibus Solicitations, and all of other SBIR/STTR solicitations on the Funding page of the SBIR/STTR Website: https://sbir.nih.gov/funding.
Be sure to also check the targeted funding announcements page, https://sbir.nih.gov/funding/individual-announcements. NIH Institutes and Centers will issue targeted SBIR/STTR grant solicitations around specific, high-priority research areas.
The next submission deadline is September 5, 2019.
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[post_content] => Two important updates regarding upcoming BARDA DRIVe funding opportunities:
Drive Special Instructions – Due May 28!
White papers, quad chart, and application form for the DRIVe special instructions to the BARDA BAA are due by 3:00 PM ET on Tuesday May 28th, 2019.
Focus areas are:
• 15.1: Advanced Research and Development of Sepsis Diagnostics and Devices
• 15.2: Post-sepsis Monitoring
• 16.1: On-Person, Wearable, and Biosensing Devices (Host Response and Direct Pathogen Detection)
Steps to apply:
1.Review Solicitation BAA-18-100-SOL-00003 on fbo.gov.
2.Schedule a meeting with the ENACT or Solving Sepsis team (strongly encouraged).
3.Download the DRIVe Special Instructions Submission Form.*
4.Complete the PDF form, Quad Chart, White Paper, and Addendum (ROM cost estimate).
5. Email your submission to DRIVeContracting@hhs.gov by 3:00PM ET on May 28th.
6. You will receive an email notification confirming receipt within 5 business days. DRIVe personnel will review your white paper as described in the solicitation.
7. DRIVe personnel will notify you of the outcome of that review and may invite you to submit a full proposal.
*You must download the PDF, as filling it out in a browser window will disable some key functionality.
General DRIVe EZ-BAA - Deadline Extended
The deadline for DRIVe’s EZ-BAA has been extended to 3:00 PM ET on November 15th, 2019. Applications are reviewed on a rolling basis with a response as early as 30 days after submission.
DRIVe has a new online portal for submitting EZ-BAA. Note: Companies must register for a profile in the online portal here, it can take up to 1 business day to account to be created.
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[post_excerpt] => DRIVe special instructions to the BARDA BAA are due by 3:00 PM ET on Tuesday May 28th! General application deadline for EZ-BAA extended until November 15th.
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[post_content] => Springboard's Health Innovation Hub is a collaboration platform advancing the growth of women-led digital health and life science companies with access to sources of funding, partnerships, and advisors. Learn more on their website, download the 1-pager, or apply here.
[post_title] => Springboard Enterprises' Health Innovation Hub
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[post_content] => Stony Brook University, iCell Gene Therapeutics and University of Louisville collaborate to offer a new CAR T immunotherapy to treat patients.
Stony Brook University, iCell Gene Therapeutics, and the University of Louisville, have received Food and Drug Administration (FDA) clearance for an Investigational New Drug (IND) for the treatment of relapsed and refractory T-cell leukemia and lymphoma. The approach is the first to use chimeric antigen receptor engineered T-cells directed against the target protein CD4 (CD4CAR). Together, Stony Brook University, the University of Louisville, and iCell Gene Therapeutics expect the first in-human Phase I clinical trial to begin accruing patients before the end of 2018.
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“The development of this trial using CD4 as a target is the first of what we expect to be many CAR T-based clinical trials available to our patients over time,” said Yusuf Hannun, MD, Director of the Stony Brook University Cancer Center. “The pending trial is an example of the type of bench-to-bedside research that is building up at Stony Brook due to the growing expertise and collaborative research environment we are creating and new opportunities that will emerge upon the opening of our Medical and Research Translation (MART) Building.”
William Tse, MD, FACP, Chief of the Blood and Marrow Transplantation at the University of Louisville School of Medicine, is the Co-PI of the CD4CAR clinical trial at University of Louisville site.
[post_title] => Client News: First In-Human Clinical Trial Targeting CD4 Protein for Aggressive T-cell Leukemia and Lymphoma to be Launched
[post_excerpt] => CFB Client iCell Gene Therapeutics, Stony Brook University, and the University of Louisville, have received FDA clearance for an Investigational New Drug (IND) for the treatment of relapsed and refractory T-cell leukemia and lymphoma.
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[post_content] => Two important updates regarding upcoming BARDA DRIVe funding opportunities:
Drive Special Instructions – Due May 28!
White papers, quad chart, and application form for the DRIVe special instructions to the BARDA BAA are due by 3:00 PM ET on Tuesday May 28th, 2019.
Focus areas are:
• 15.1: Advanced Research and Development of Sepsis Diagnostics and Devices
• 15.2: Post-sepsis Monitoring
• 16.1: On-Person, Wearable, and Biosensing Devices (Host Response and Direct Pathogen Detection)
Steps to apply:
1.Review Solicitation BAA-18-100-SOL-00003 on fbo.gov.
2.Schedule a meeting with the ENACT or Solving Sepsis team (strongly encouraged).
3.Download the DRIVe Special Instructions Submission Form.*
4.Complete the PDF form, Quad Chart, White Paper, and Addendum (ROM cost estimate).
5. Email your submission to DRIVeContracting@hhs.gov by 3:00PM ET on May 28th.
6. You will receive an email notification confirming receipt within 5 business days. DRIVe personnel will review your white paper as described in the solicitation.
7. DRIVe personnel will notify you of the outcome of that review and may invite you to submit a full proposal.
*You must download the PDF, as filling it out in a browser window will disable some key functionality.
General DRIVe EZ-BAA - Deadline Extended
The deadline for DRIVe’s EZ-BAA has been extended to 3:00 PM ET on November 15th, 2019. Applications are reviewed on a rolling basis with a response as early as 30 days after submission.
DRIVe has a new online portal for submitting EZ-BAA. Note: Companies must register for a profile in the online portal here, it can take up to 1 business day to account to be created.
[post_title] => DRIVe Special Instructions & EZ-BAA Updates
[post_excerpt] => DRIVe special instructions to the BARDA BAA are due by 3:00 PM ET on Tuesday May 28th! General application deadline for EZ-BAA extended until November 15th.
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