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ACADIA PHARMACEUTICALS INC

Parent1 subsidiaryUEI: D79ND8GZR3E6CAGE: 5LB84

ACADIA PHARMACEUTICALS INC is a federal contractor, registered under UEI D79ND8GZR3E6 and CAGE code 5LB84. It has been awarded $600,000 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

D79ND8GZR3E6

CAGE Code

5LB84

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

Acadia Pharmaceuticals Inc. specializes in the manufacturing of pharmaceutical preparations, with a focus on developing and supplying specialized drugs, including those used in hematology and related therapeutic areas. The company leverages advanced pharmaceutical formulation technologies to produce...

Acadia Pharmaceuticals Inc. specializes in the manufacturing of pharmaceutical preparations, with a focus on developing and supplying specialized drugs, including those used in hematology and related therapeutic areas. The company leverages advanced pharmaceutical formulation technologies to produce high-quality, regulated drug products compliant with federal standards for safety, efficacy, and consistency. Their technical expertise encompasses active pharmaceutical ingredient processing, aseptic manufacturing, batch control systems, and supply chain integrity for government-distributed medications. As a manufacturer operating under strict FDA oversight, they ensure adherence to cGMP protocols and maintain rigorous quality assurance frameworks essential for federal procurement. The company has demonstrated direct engagement with the Department of Veterans Affairs, providing pharmaceutical products under Federal Supply Schedule contracts, indicating a trusted relationship in supporting veteran healthcare needs through reliable drug procurement channels. This partnership suggests familiarity with VA’s formulary requirements, distribution logistics, and the unique pharmacological needs of veteran populations, including chronic disease management and specialty therapeutics. Acadia’s primary industry focus is in NAICS 325412, which encompasses the manufacturing of finished pharmaceutical dosage forms such as tablets, capsules, injectables, and other standardized drug products. Their market positioning centers on specialty pharmaceutical manufacturing for government healthcare systems, distinguishing themselves through precision production of complex or high-demand therapeutics used in clinical care settings. As a privately held entity structured as a 2L corporation based in San Diego, California, Acadia Pharmaceuticals Inc. operates without federal small business certifications. Their geographic footprint is anchored in Southern California, a hub for biopharmaceutical innovation, enabling proximity to research institutions and supply chain partners critical to federal pharmaceutical delivery. The company’s government market presence is defined by direct product supply rather than service-based contracting, positioning them as a reliable manufacturer within the federal drug procurement ecosystem.

Key performance metrics

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

Awards Count

8

All time · Whole family

Active

0

Currently performing · Whole family

Completed

8

Past period of performance · Whole family

Total Awards

All time · Whole family

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

Subsidiaries

1 company rolls up into ACADIA PHARMACEUTICALS INC, sized by each one's own awards

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Open opportunities in ACADIA PHARMACEUTICALS INC's top NAICS codes and agencies

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

6 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

6 months ago

DEADLINE

in 5 months
View Details
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

6 months ago

DEADLINE

in 5 months
View Details