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Enroll Your Immuno-Oncology Agents in Our Next MuScreen™ Today

MuScreen is the first high throughput in vivo screen for evaluating immunotherapy and immune modulating compounds across both well-characterized syngeneic and unique tumor homograft models.

Agent efficacy is evaluated using syngeneic and/or tumor homograft model panels, with PD effects assessed using syngeneic models only. MuScreen is a cost-effective screening platform, with a free vehicle arm and shared cost of the positive control arm.

Select the Models and Study Design to Suit Your Program

Model Type Model  Features
Efficacy PD
US
China
US
China
Syngeneic Display immune heterogeneity
and diversity observed
in the clinic
6
models
6
models
12
models
Tumor Homograft   Transplants of GEMM tumors
into a syngeneic host, preserving
original GEMM tumor molecular
and histopathology and clinically
relevant oncogenic driver mutations
  6
models
   


MuScreen Schedules

Syngeneic

12 Model Efficacy and PD Mode
Study Site: Crown Bioscience China
Registration Deadline
Study Initiation
January 12th, 2024
March 1st, 2024
April 19th, 2024
May 17th, 2024
July 12th, 2024
August 9th, 2024
September 13th, 2024
October 18th, 2024
 
6 Model Syngeneic Efficacy and PD Mode
Study Site: Crown Bioscience San Diego
Registration Deadline
Study Initiation
January 12th, 2024
March 1st, 2024
April 19th, 2024
May 17th, 2024
July 12th, 2024
August 9th, 2024
September 13th, 2024
October 18th, 2024

Tumor Homograft

6 Model Efficacy Mode
Study Site: Crown Bioscience China
Registration Deadline
Study Initiation
January 12th, 2024
March 1st, 2024
May 10th, 2024
June 21st, 2024
September 6th, 2024
October 18th, 2024



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