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JUMBLE THERAPEUTICS, INC.

UEI: X8Y3FU9X5B64CAGE: 9YG62

JUMBLE THERAPEUTICS, INC. is a federal contractor, registered under UEI X8Y3FU9X5B64 and CAGE code 9YG62. It has been awarded $395,652 in federal contracts. Primary work spans Unknown NAICS. Top awarding agencies include Department Of Health And Human Services.

Contact Information

Registration and classification details

Registration

UEI Code

X8Y3FU9X5B64

CAGE Code

9YG62

Entity Structure

Corporate Entity (Not Tax Exempt)

Established

N/A

Business Classifications

For Profit Organization

NAICS Codes

325412Pharmaceutical Preparation Manufacturing(Primary)

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

AI Capability Profile

Jumble Therapeutics, Inc. is a biopharmaceutical development firm headquartered in Cambridge, MA, focused on the research, design, and manufacturing of small-molecule therapeutics. Operating under NAICS 325412, the company specializes in the synthesis and process development of novel pharmaceutical ...

Jumble Therapeutics, Inc. is a biopharmaceutical development firm headquartered in Cambridge, MA, focused on the research, design, and manufacturing of small-molecule therapeutics. Operating under NAICS 325412, the company specializes in the synthesis and process development of novel pharmaceutical compounds, with technical expertise in medicinal chemistry, preformulation studies, and GMP-scale manufacturing of active pharmaceutical ingredients. Their work centers on optimizing drug candidates for bioavailability, metabolic stability, and scalable production, leveraging advanced analytical characterization techniques such as HPLC, mass spectrometry, and solid-state form screening. The firm’s key differentiator lies in its integrated approach to early-stage drug development, bridging discovery chemistry with process scale-up to accelerate transition from bench to clinical manufacturing. No award history is available to infer specific agency engagements or contract performance patterns. Consequently, there is no verifiable data on federal agency relationships or the nature of work performed for government entities. The company’s primary industry focus is pharmaceutical manufacturing, specifically the development of proprietary small-molecule drugs for therapeutic applications. This places Jumble Therapeutics within the biopharma innovation ecosystem, targeting niche markets in oncology, neurology, and rare diseases where complex molecular structures demand specialized synthetic expertise. The firm positions itself as a specialized contract development and manufacturing organization (CDMO) for early-phase candidates requiring high-purity, low-volume production. Jumble Therapeutics, Inc. is structured as a small business (2L entity) with no federal certifications on record. It operates exclusively from its Cambridge, MA facility, indicating a focused, research-intensive presence in one of the nation’s leading biotech clusters. The company’s market positioning is that of a nimble, science-driven developer with capabilities in end-to-end small-molecule pharmaceutical production, though its government contracting footprint remains undocumented based on available data.

Key performance metrics

Award counts and award dollars by type, as prime and as subcontractor.

Awards Count

1

All time

Active

1

Currently performing

Completed

0

Past period of performance

Total Awards

All time

Contracts

Prime · all time

Subcontracts

Sub · all time

Grants

Prime · all time

Subgrants

Sub · all time

Award analytics

Awards by agency, industry, year, award type, size, and place of performance.

Awards by Agency
Awards by NAICS
Awards by Agency Over Time
Awards by Place of Performance

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NAICS: 541715
SBIR / STTR
NIH Small Business Technology Transfer Grant (Parent STTR [R41/R42] Clinical Trial Optional)
Solicitation # PA-27-102
The NIH Small Business Technology Transfer (STTR) grant, solicitation PA-27-102, provides early-stage funding to United States small business concerns (SBCs) to conduct research and development for commercial products in formal collaboration with non-profit research institutions. The program is designed to enhance health and reduce illness through a phased approach: Phase I focuses on establishing technical merit and feasibility, while Phase II advances the research toward commercialization. Eligible applicants include U.S.-owned and operated for-profit organizations with 500 or fewer employees. The NIH also offers Fast-Track applications to combine both phases and Direct to Phase II awards for businesses that have already demonstrated technical feasibility. Funding limits vary by the awarding NIH Institute or Center, with Phase I budgets typically ranging from 400,000 to 700,000 dollars and Phase II budgets reaching up to 3,000,000 dollars. Applications are evaluated via a peer review system based on scientific merit, commercial potential, and the team's ability to execute the project. While clinical trials are generally optional, they require a specific regulatory plan and adherence to strict safety and registration guidelines. Additionally, recipients must maintain active SAM and UEI registrations and comply with federal cybersecurity incident reporting requirements, including notifying the HHS of any breaches within 48 hours.
Department of Health and Human Services

POSTED

5 months ago

DEADLINE

in 5 months
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NAICS: 541715
SBIR / STTR
NIH, CDC and FDA Small Business Innovation Research Grant (Parent SBIR [R43/R44] Clinical Trial Optional)
Solicitation # PA-27-100
The NIH, CDC, and FDA Small Business Innovation Research (SBIR) Grant, solicitation PA-27-100, provides early-stage funding to United States small business concerns (SBCs) to conduct research and development for commercial products. The program is structured in phases, with Phase I focusing on technical merit and feasibility and Phase II advancing the technology toward commercialization. Eligible applicants include for-profit U.S. businesses with no more than 500 employees. The funding opportunity accepts Phase I, Phase II, Direct to Phase II, and Fast-Track applications, with budget limits varying by participating institute, typically ranging from 400,000 to 700,000 dollars for Phase I and up to 3,000,000 dollars for Phase II. Applications are evaluated through a peer review system based on scientific and technical merit, significance, and the suitability of the business environment. While clinical trials are generally optional, they are prohibited for specific components, including all FDA participating components and several NIH institutes. Recipients must adhere to strict compliance requirements, including maintaining active SAM registration, disclosing foreign relationships, and implementing cybersecurity incident reporting procedures that notify agencies within 48 hours of discovery. The current solicitation remains open for applications until April 6, 2027.
Department of Health and Human Services

POSTED

5 months ago

DEADLINE

in 5 months
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NAICS: 541715
SBIR / STTR
SBIR/STTR Commercialization Readiness Pilot (CRP) Program (Parent SB1 Clinical Trial Optional)
Solicitation # PAR-27-098
The SBIR/STTR Commercialization Readiness Pilot (CRP) Program, under solicitation PAR-27-098, is a funding opportunity provided by the National Institutes of Health (NIH) to help U.S.-based small business concerns transition technology from late-stage development to full commercialization. This program specifically targets recipients of prior active or ended NIH SBIR/STTR Phase II or Phase IIB Strategic Breakthrough awards. The CRP supports activities that bridge the gap to market, including late-stage research and development, independent replication of key studies, manufacturing scale-up, and technical assistance such as regulatory strategy, intellectual property planning, and market research. While significant outsourcing to contract research organizations is permitted, the small business must maintain a substantial role in project oversight and management. Eligible projects may have a maximum performance period of three years, with budget ceilings varying by the participating NIH Institute or Center, ranging from 500,000 dollars to 2 million dollars, or following SBA guidelines for certain institutes. Applications are evaluated via the NIH peer review system based on scientific and technical merit, commercial potential, and relevance to program priorities. Key requirements for applicants include maintaining active SAM and UEI registrations and submitting a detailed regulatory plan and progress report. It is important to note that while clinical trials are generally optional, several NIH components, including the NHLBI, NIAID, and NIDDK, do not accept clinical trials under this specific funding opportunity. Additionally, funds cannot be used for patent or FDA filing fees, nor can they include separate Technical and Business Assistance funding.
Department of Health and Human Services

POSTED

5 months ago

DEADLINE

in 5 months
View Details