Clinical trial • Phase I • Oncology

CC-1 (PSMAxCD3 bispecific antibody) for Recurrent prostate cancer

Phase I trial of CC-1 (PSMAxCD3 bispecific antibody) for Recurrent prostate cancer. None/Not specified-controlled. 56 participants.

Overview

Trial Therapeutic Area
Oncology
Trial Disease
Recurrent prostate cancer
Trial Stage
Phase I
Drug Modality
Bispecific antibody

Key dates

Initial CTIS Submission Date
12-02-2024
First CTIS Authorization Date
05-03-2024

Trial design

None/Not specified-controlled Phase I trial across 1 site in Germany.

Comparator
None/Not specified
Target Sample Size
56

Eligibility

Recruits 56 Vulnerable population not selected; no special consent or assent handling is described in the available documentation..

Vulnerable Population
Vulnerable population not selected; no special consent or assent handling is described in the available documentation.

Recruitment

Planned Sample Size
56
Recruitment Window Months
49
Consent Approach
Informed consent obtained from adult participants; no vulnerable populations selected; no details on assent, age-specific documents, or languages available in the provided records.

Geography

Total Number Of Sites
1
Total Number Of Participants
56

Germany

Earliest CTIS Part Ii Submission Date
01-02-2024
Latest Decision Or Authorization Date
26-03-2025
Processing Time Days
419
Number Of Sites
1
Number Of Participants
56

Sites

Site Name
Universitaetsklinikum Tuebingen AöR
Department Name
KKE Translationale Immunologie
Contact Person Name
Juliane Walz
Contact Person Email
kketi@med.uni-tuebingen.de
Number Of Participants
56

Sponsor

Primary sponsor

Full Name
Universitaetsklinikum Tuebingen AöR
Organisation Type
Hospital/Clinic/Other health care facility
Country Of Registered Address
Germany

Investigational products

Investigational Product Name
CC-1
Active Substance
CC-1 (PSMAxCD3 bispecific antibody)
Modality
Bispecific antibody

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