ISRCTN ISRCTN79202365
DOI https://doi.org/10.1186/ISRCTN79202365
Integrated Research Application System (IRAS) 1013718
CRO code QSC302725
Sponsor Agomab Spain, S.L.U.
Funder Agomab Spain, S.L.U.
Submission date
23/06/2026
Registration date
23/06/2026
Last edited
23/06/2026
Recruitment status
Not yet recruiting
Overall study status
Deferred
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

This is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.

Contact information

Dr Litza McKenzie
Principal investigator

Quotient Sciences Limited
Mere Way
Ruddington Fields
Ruddington
Nottingham
NG11 6JS
United Kingdom

Phone +44 (0)3303031000
Email recruitment@weneedyou.co.uk
Clinical Operations, Agomab Spain, S.L.U.
Scientific, Public

Parque Empresarial De Touro, Parcelas 26-27, Fonte Diaz
A Coruña
15822
Spain

Phone +32 33189170
Email clinicalstudies@agomab.com

Study information

Primary study designInterventional
AllocationN/A: single arm study
MaskingOpen (masking not used)
ControlUncontrolled
AssignmentSingle
PurposePhase I trial in healthy volunteers
Scientific titleDeferred registration: Quotient Sciences Code: QSC302725 [Full scientific title to be added on or before the deferral expiry date]
Study objectives This is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Ethics approval(s)

Approved 11/06/2026, London - Brent Research Ethics Committee (Health Research Authority, 2 Redman Place, Stratford, London, E20 1JQ, United Kingdom; +44 (0)20 7104 8128; brent.rec@hra.nhs.uk), ref: 26/LO/0189

Health condition(s) or problem(s) studiedHealthy volunteers
InterventionThis is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Intervention typeDrug
PhasePhase I
Drug / device / biological / vaccine name(s)This is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Primary outcome measure(s)
  1. [Outcome name] measured using [Metric or method of measurement] at [Timepoint(s)]. This is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Key secondary outcome measure(s)
Completion date06/08/2026

Eligibility

Participant type(s)
Age groupMixed
Lower age limit30 Years
Upper age limit65 Years
SexMale
Target sample size at registration8
Key inclusion criteriaThis is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Key exclusion criteriaThis is a phase I trial in healthy volunteers only and qualifies for an automatic deferral. The full details will be added to the trial record on or before the deferral expiry date.
Date of first enrolment24/06/2026
Date of final enrolment06/08/2026

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Quotient Sciences Limited
Mere Way
Ruddington Fields
Ruddington
Nottingham
NG11 6JS
England

Results and Publications

Individual participant data (IPD) Intention to shareNo

Editorial Notes

23/06/2026: Trial's existence confirmed by MHRA.