<?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="2026-06-22T07:57:45Z" ns1:href="http://gtr.ukri.org/gtr/api/projects/C907E581-35CD-4F76-BB88-E54D5952B5F7" ns1:id="C907E581-35CD-4F76-BB88-E54D5952B5F7"><ns1:links><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/persons/72B3D1F1-F1F4-4D98-A47B-874A5CDFF5A2" ns1:rel="PM_PER"/><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/organisations/81E3C9FA-D77C-4103-A923-E2CE6BDFBB1C" ns1:rel="LEAD_ORG"/><ns1:link ns1:href="http://gtr.ukri.org/gtr/api/organisations/81E3C9FA-D77C-4103-A923-E2CE6BDFBB1C" ns1:rel="PARTICIPANT_ORG"/><ns1:link ns1:end="2018-03-30T23:00:00Z" ns1:href="http://gtr.ukri.org/gtr/api/funds/88AE7855-6DA4-43D4-B780-025AECB400CA" ns1:rel="FUND" ns1:start="2014-11-01T00:00:00Z"/></ns1:links><ns2:identifiers><ns2:identifier ns2:type="RCUK">101872</ns2:identifier></ns2:identifiers><ns2:title>Clinical Development of OXB-102</ns2:title><ns2:status>Closed</ns2:status><ns2:grantCategory>Collaborative R&amp;D</ns2:grantCategory><ns2:leadFunder>Innovate UK</ns2:leadFunder><ns2:abstractText>Parkinson's disease is caused by the degeneration of nerve cells in part of the brain; leading to the loss of dopamine, a chemical messenger which plays a vital role in coordinating body movement. In early stages of PD, oral levadopa (L-DOPA) medication is effective in managing the symptoms that include tremor, muscle stiffness and slow physical movement. However, the body progressively loses its ability to convert L-DOPA to dopamine thereby reducing its effectiveness and leading to the development of uncontrolled motor function. Oxford BioMedica has developed a 'once-only' gene therapy approach to treat individuals with PD called OXB-102 that is administered once to the target region in the brain where it converts cells into a replacement dopamine factory. In essence, OXB-102 replaces a patient’s own lost source of the neurotransmitter analogous to the natural dopamine supply in the absence of PD.</ns2:abstractText></ns2:project>