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The DEPT. OF THE ARMY -- USAMRAA has issued a Tender notice for the procurement of a Dow Amyotrophic Lateral Sclerosis Research Program, Pilot Clinical Trial Award in the USA. This Tender notice was published on 05 May 2026 and is scheduled to close on 30 Sep 2026, with an estimated Tender value of Refer Document. Interested bidders can access detailed Tender information, eligibility criteria, and complete bidding documents by referencing TOT Ref No. 140656221, while the tender notice number is HT942526ALSRPPCTA and Registering on the platform.
Procurement Summary
Country: USA
Summary: Dow Amyotrophic Lateral Sclerosis Research Program, Pilot Clinical Trial Award
Deadline: 30 Sep 2026
Posting Date: 05 May 2026
Other Information
Notice Type: Tender
TOT Ref.No.: 140656221
Document Ref. No.: HT942526ALSRPPCTA
Competition: ICB
Financier: Self Financed
Purchaser Ownership: Public
Tender Value: Refer Document
CPV Classification
48814400 - Clinical information systemPurchaser's Detail
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Email: Login to see tender_detailsLogin to see details Tender Details Summary: The Fiscal Year 2026 (Fy26) Amyotrophic Lateral Sclerosis Research Program (Alsrp) Pilot Clinical Trial Award (Pcta) Supports The Rapid Implementation Of Clinical Trials With The Potential To Have A Significant Impact On The Treatment Or Management Of Amyotrophic Lateral Sclerosis (Als). Projects May Range From Phase 1 To Small-Scale Phase 2 Trials.Applications Must Address One Of The Following Focus Areas:· Biomarker-Driven Interventions: Disease-Modifying Interventions, With Mechanism-Specific Biomarkers To Predict Which Clinical Trial Participants Are Likely To Respond, Demonstrate Target Engagement, And Effects On The Intended Biological Pathway.· Clinical Care: Improving Aspects Of Clinical Care And Symptom Management For Als.Distinctive Features: Funding From This Award Mechanism Must Support A Clinical Trial. The Clinical Trial Should Begin No Later Than 12 Months After The Award Date Or 18 Months For U.S. Food And Drug Administration (Fda)-Regulated Studies.Projects Proposing A Therapeutic Intervention (Drug, Biologic, And/Or Device) Must Incorporate Biomarkers Specific To The Intervention Into The Trial Design.All Pre-Applications And Applications Are Required To Incorporate Community Collaboration, As Described In Section 3.2.2, To Optimize Research Impact.Applications Must Include A Detailed Regulatory Strategy Plan That Outlines The Approach For Obtaining Regulat... Documents
Posted Date: 2026-05-04 00:00:00
Funding instrument type: Grant
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