<?xml version="1.0" encoding="UTF-8"?><ns2:project xmlns:ns1="http://gtr.rcuk.ac.uk/gtr/api" xmlns:ns2="http://gtr.rcuk.ac.uk/gtr/api/project" xmlns:ns3="http://gtr.rcuk.ac.uk/gtr/api/fund" xmlns:ns4="http://gtr.rcuk.ac.uk/gtr/api/person" xmlns:ns5="http://gtr.rcuk.ac.uk/gtr/api/project/outcome" xmlns:ns6="http://gtr.rcuk.ac.uk/gtr/api/organisation" ns1:created="2026-07-08T08:44:08Z" ns1:href="http://gtr.ukri.org/gtr/api/projects/EB309FAB-1B55-4A16-8991-237414BDC986" ns1:id="EB309FAB-1B55-4A16-8991-237414BDC986"><ns1:links><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/persons/4FFF6607-28EE-4B8E-8131-5B462EA1CECC" ns1:rel="PM_PER"/><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/organisations/3C26DF17-881E-4E2A-B8D9-7499CE0F79C1" ns1:rel="LEAD_ORG"/><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/organisations/3C26DF17-881E-4E2A-B8D9-7499CE0F79C1" ns1:rel="PARTICIPANT_ORG"/><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/organisations/8F5EFF7A-52BF-4624-A251-84DFAD4CD84E" ns1:rel="PARTICIPANT_ORG"/><ns1:link ns1:end="2023-12-31T00:00:00Z" ns1:href="http://gtr.ukri.org/gtr/api/funds/46CC1F58-5E56-4B9E-9249-572AE6170645" ns1:rel="FUND" ns1:start="2021-01-01T00:00:00Z"/></ns1:links><ns2:identifiers><ns2:identifier ns2:type="RCUK">74975</ns2:identifier></ns2:identifiers><ns2:title>OsteoMiR -- a novel disease-modifying drug for the treatment of osteoarthritis.</ns2:title><ns2:status>Closed</ns2:status><ns2:grantCategory>Study</ns2:grantCategory><ns2:leadFunder>UKRI Inn.Scholar</ns2:leadFunder><ns2:abstractText>Osteoarthritis (OA) is the leading cause of disability in older adults with 1 in 8 being affected. Around 75% of people with OA report constant pain, with approximately 30% giving up work or reducing the number of hours they work due to the condition. The cost of OA in the USA and Europe has been estimated at 1-2.5% of GDP. Currently, there are no Disease-Modifying OA Drugs (DMOAD). Loss of cartilage is believed to be a major cause of osteoarthritis symptoms and therefore, therapies that limit or reverse this damage are likely to reduce symptoms and benefit patients. Causeway Therapeutics is developing a treatment that uniquely targets the cellular pathways that drive the development of OA stopping disease progression, restoring function and reducing pain.</ns2:abstractText></ns2:project>