SBIR/STTR Research Award

Recombinant botulinum toxin with improved safety and effectiveness for treatment of dystonia

Award identifier 21841222cbc52ad7ffb4a5d7f477ea593f1ced4eabe1c1ab5b364c32ab97b6c5Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$414,924

Program and phase

SBIR · Phase I

Award year

2022

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Cytodel, Inc.
Proposal award date
2022-03-01
Contract end date
2023-08-31
UEI
LSDWPNU9NAC9
Solicitation number
PA20-260
Topic code
106

Research abstract

Abstract Botulinum neurotoxin (BoNT) is the most toxic protein known to science. It is also the active ingredient in® pharmaceutical products like Botox (Allergan), which have proven safe and effective for multiple neuromuscular indications. All current BoNT products are manufactured from Clostridium botulinum cultures and have similar safety characteristics, which include limitations on dosing and a black box warning in labeling. Because of its inherent toxicity and narrow therapeutic window, optimal clinical outcomes are difficult to achieve in indications involving large muscle groups, such as cervical dystonia, post-stroke spasticity and pediatric cerebral palsy. Though improved muscle tone can clearly be achieved, clinicians tend to dose on the side of caution, and overall clinical outcomes leave significant room for improvement. We here propose building on data generated with a previous candidate for a “safer BoNT” pharmaceutical (SBIR Phase 1 1R41NS086115-01A1) which found that specific amino acid substitutions to BoNT/A1 can produce a recombinant BoNT/A1 with an improved safety margin compared to wt BoNT/A1, (US 8,865,186). The initial lead candidate designed and tested, Cyto-012, had an improved safety margin, but its absolute potency was such that doses required for efficacy were also immunogenic. Here, we propose testing a new recombinant BoNT/A1 derivative termed Cyto-014, designed to have potency and immunogenicity similar to wt BoNT/A1, while retaining the desired improvement in safety suggested by our Preliminary Studies. This proposal is intended to compare the dose-response behavior, safety margin and maximum tolerated dose of Cyto-014 relative to wt BoNT/A1 in appropriately powered studies, and to evaluate its immunogenicity and effectiveness for repeat treatment. Successful completion of the proposed studies will support a Phase II study to focus on pre-clinical development activities aimed at filing an IND.

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 (2014–2023). Reported award amounts total $934,229. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.