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Manufacture and testing of overencapsulated tablets and placebo capsules for research purposes - LAMDARCT clinical trial

Belfast Health & Social Care Trust

Buyer Contact Info

Buyer Name: Belfast Health & Social Care Trust

Buyer Address: Trust Headquarters, 2nd Floor, Non Clinical Support Building, Royal Victoria Hospital, Belfast, UKN06, BT12 6BA, United Kingdom

Contact Email: FinanceProcurement@belfasttrust.hscni.net

Status
complete
Procedure
direct
Value
494447.5 GBP
Published
21 Jan 2026, 09:15
Deadline
n/a
Contract Start
19 Jan 2026, 00:00
Contract End
05 Jan 2030, 23:59
Category
n/a
CPV
33600000 - Pharmaceutical products
Region
n/a
Awarded To
ALMAC CLINICAL SERVICES LIMITED
Official Source
Open Find a Tender

Description

This procurement is for the manufacture and testing of over encapsulated tablets and placebo capsules for research purposes - LAMDARCT clinical trial

Linked Documents

No linked documents found for this notice.

Opportunity Context

Lots

Lot 1 Status: complete

Documents

Document Description: Not published

Contracts

Contract Title: Manufacture and testing of overencapsulated tablets and placebo capsules for research purposes - LAMDARCT clinical trial

Raw Notice JSON

Expand raw payload
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    "procurementMethodRationale": "Schedule 5, (2) The public contract concerns the production of a prototype, or supply of other novel goods or services, for the purpose of (c) other research, experiment, study or development.\nAge-related macular degeneration (AMD) is a leading cause of visual loss. There are two main forms of AMD: dry and wet. The current wet AMD treatment is intravitreal antiVEGF injections, repeated every 4-12 weeks. Due to the cost of the medication, the route and frequency of administration, this treatment is a significant burden on the NHS budget. An additional treatment option for wet AMD is L-dopa. L-dopa is a widely available drug (used in treatment of Parkinson\u0027s), typically in the form of Carbidopa-L-Dopa. It is taken as an oral tablet and is significantly cheaper than the antiVEGF injections.\nThe study will be a placebo-controlled clinical trial. Eligible patients will be randomised to receive either 100mg L-DOPA+25mg carbidopa or placebo twice a day, for 24 months, in addition to the current standard of care to determine if this is a more cost-effective and easier-to-administer treatment regime than the current standard of care. \nTo \u0027blind\u0027 this clinical trial (to reduce bias) requires the development, manufacture and testing of over encapsulated 100mg L-DOPA+25mg carbidopa tablets and development and manufacture of matching placebo capsules. The expertise required to develop and manufacture these capsules in the quantity required for this trial requires outsourcing to a manufacturer licensed by the MHRA possessing the necessary technical expertise.",
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