Recent Updates
Recently added Catalysts

BED003

Phase 2

Colorectal Cancer | Small molecule | Other |Medpace Holdings, Inc. Common Stock|Last Updated: Sep 15, 2026

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLEDBiomarker
Total Trials1
Total Enrollment71

FDA Designations

No designations recorded

Clinical trial landscape

BED003 · 1 trial · 5 indications

Phase 2 1
NCT07702292[68Ga]BED003 PET Imaging of Fibroblast Activation Protein in Selected Oncology IndicationsColorectal Cancer
RECRUITING71 Analytics
PHASE2RECRUITING
[68Ga]BED003 PET Imaging of Fibroblast Activation Protein in Selected Oncology Indications
Colorectal CancerUnlock trial analytics

Study Endpoints

Primary Endpoints

Assess the diagnostic performance of [68Ga]BED003 in the peritoneum.
Until completion of follow-up procedures, up to 42 days post injection.

Assess the diagnostic performance of \[68Ga\]BED003 in the peritoneum.

Secondary Endpoints

Further assess the diagnostic performance of [68Ga]BED003.
Until completion of follow-up procedures, up to 42 days post injection
Semiquantitative assessment of [68Ga]BED003 tumour uptake.
Immediately following administration of [68Ga]BED003
Evaluate the safety and tolerability of [68Ga]BED003.
From screening until safety follow-up (48 hours post injection).
Unlock Study Endpoints

Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeDIAGNOSTIC

Treatment Arms

ArmTypeDescription
[68Ga]BED003EXPERIMENTALEach participant will receive \[68Ga\]BED003 followed by positron emission tomography (PET)/computed tomography (CT) imaging at the PET/CT imaging visit (Visit 2).

Interventions

NameTypeDescription
[68Ga]BED003DRUGPositron emission tomography (PET)/computed tomography (CT) imaging
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to 79 Years
SexALL
Healthy VolunteersNo
Study Sites6

Inclusion Criteria: 1. Participants provide informed consent and confirm that they are able and willing to comply with all protocol requirements. 2. Participants must be ≥ 18 years and \< 80 years of age and competent to give informed consent. 3. Eastern Cooperative Oncology Group performance statu...

Countries:ItalyNetherlands
Unlock Eligibility Criteria

Competitive Landscape -Colorectal Cancer 257 trials