- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06842407
Novel Targets for the Development of Monoclonal Antibodies for Immunotherapy) (Immuno-ab)
February 19, 2025 updated by: Checkmab S.r.l.
Nuovi Bersagli Per lo Sviluppo di Anticorpi Monoclonali Per Immunoterapia - (Novel Targets for the Development of Monoclonal Antibodies for Immunotherapy)
The first objective of the project consists in the preclinical validation of new possible molecular targets associated with intratumoral T regulatory cells.
The second objective consists in the selection of monoclonal antibodies with therapeutic potential, specific for the selected targets.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
600
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Renata M Grifantini, PhD
- Phone Number: 0039 00660220
- Email: renata.grifantini@checkmab.eu
Study Locations
-
-
-
Milan, Italy, 20122
- Recruiting
- S.C. Medicina Trasfusionale - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
-
Contact:
- Daniele Prati, MD
- Phone Number: 0039 0255034687
- Email: daniele.prati@policlinico.mi.it
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Healthy subjects
Description
Inclusion Criteria:
- blood donors
- age of 18 years or more
- able to sign informed consent
Exclusion Criteria:
- age below 18 years
- Positive for HIV, HCV, HBV
- not suitable for blood donation
- not able to understand or sign informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Healthy Donors
subjects over 18 years of age
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Validation of molecular targets for immunotherapy
Time Frame: 04.2023-06.2026
|
04.2023-06.2026
|
|
Selection of therapeutic antibodies
Time Frame: 04.2023-06.2026
|
04.2023-06.2026
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Set up of immunological assays to adress monoclonal antibodies mechanism of action
Time Frame: 04.2023-06.2026
|
04.2023-06.2026
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2023
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
June 30, 2026
Study Registration Dates
First Submitted
February 14, 2025
First Submitted That Met QC Criteria
February 19, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 19, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- ID3411
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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