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In Vivo Screen for APC/β-Catenin Dysregulation

Choose from 31 PDX models covering colorectal, endometrial, esophagael, gastric, melanoma, NSCLC and ovarian cancer, to advance your preclinical compounds.

Enrollment deadline: Enrolling until March 27th, 2026

Request more information on our In Vivo Screen for APC/β-Catenin Dysregulation

Test your small molecules, biologics, ADCs, and rational combinations targeting the APC/β‑catenin pathway.

Aberrations in the APC/β‑catenin (Wnt) pathway drive tumor initiation, progression, and therapeutic resistance across multiple solid tumors. Champions’ upcoming multi‑indication screen lets your team quickly pressure‑test mechanisms acting on this pathway, de‑risking go/no‑go decisions and informing indication strategy with in vivo evidence generated in clinically relevant PDX models.

  • Purpose‑built for APC/β‑catenin dysregulation
    The panel is enriched for tumors with APC/CTNNB1/AXIN1 alterations or pathway activation, enabling mechanism‑aligned testing and biomarker discovery
  • High translational value
    Across large, independent comparisons of PDX responses vs. subsequent patient outcomes, Champions PDX have shown 85% PPV and 91% NPV, supporting high translational confidence.
  • Seven tumor types
    Featuring 15 colorectal, 4 NSCLC, 3 esophageal, 3 melanoma, 2 endometrial, 2 gastric and 2 ovarian cancer models, with mutations such as KRAS, TP53, PIK3CA and more.
  • Collaborative Standard-of-Care arm
    Comparator context via an optional standard‑of‑care cost‑share arm, facilitating internal and external benchmarking.
  • Optional multi-omics
    By request, you can leverage multi‑omics (RNA‑seq, WES) and IHC panels (e.g., β‑catenin localization), through our established profiling workflows across our preclinical platforms.
  • Multiple efficacy readouts
    Tumor volume kinetics, TGI, response categorization plus tolerability and body‑weight monitoring, delivered in publication‑ready figures and raw data files.

Model Overview

Choose from 31 PDX models covering colorectal, endometrial,
esophagael, gastric, melanoma, NSCLC and ovarian cancer

Model
Tumor type
Mutations
Expression
Suggested SoCs
CTG-0081
Colorectal
TP53
None
FOLFIRI or FOLFOX
CTG-0148
Gastric
PIK3CA
MLH-low
Alpelisib
CTG-0387
Colorectal
KRAS G12C
None
Daraxonrasib; Sotorasib
CTG-0497
Colorectal
PIK3CA
CDK4-high
Alpelisib
CTG-0654
Colorectal
KRAS G12D
PTEN-low
Daraxonrasib; Sotorasib; Alpelisib
CTG-0661
Colorectal
KRAS G12S
CDK4-high
Daraxonrasib; Sotorasib; Palbo
CTG-0676
Esophageal
ERBB2
None
Trastuzumab deruxtecan; Trastuzumab emtansine
CTG-0812
Colorectal
None
CDK4-high; ERBB3-high
Palbociclib
CTG-0835
Colorectal
KRAS G13D; PIK3CA
None
Daraxonrasib; Sotorasib; Alpelisib
CTG-0951
Colorectal
KRAS G13D; BRCA2
AKT2-high
Daraxonrasib; Sotorasib
CTG-1170
Colorectal
KRAS G12V
None
Daraxonrasib; Sotorasib; Trastuzumab deruxtecan
CTG-1280
Endometrial
PTEN
CDK4-high; MLH1-low
Datopotamab; Sacituzumab; Alpelisib; Palbociclib
CTG-1423
Ovarian
PIK3CA
FGFR1-high
Alpelisib; Capivasertib
CTG-1471
Melanoma
None
CDK4-high; CCND1-high
Palbociclib; Binimetinib
CTG-1472
Colorectal
KRAS G12V; PIK3CA
None
Daraxonrasib; Sotorasib
CTG-1553
Colorectal
KRAS G12V
CDK4-high
Daraxonrasib; Sotorasib
CTG-1677
Ovarian
BRAF; PTEN
None
Vemurafenib; Palbociclib
CTG-1741
Esophageal
None
CCND1-high
Palbociclib
CTG-1762
NSCLC
None
FGFR1-high; CDK4-high
Trametinib; Avutometinib; Palbociclib
CTG-1876
Esophageal
TP53
None
Zongertinib; Zanidatamab; Disitamab
CTG-1951
Colorectal
KRAS G12D
None
Daraxonrasib; Sotorasib
CTG-2164
Colorectal
KRAS G12V; PIK3CA
CDK4-high
Daraxonrasib; Sotorasib
CTG-2556
NSCLC
PTEN
CDK4-high
Alpelisib; Trametinib; Avutometinib
CTG-2647
Endometrial
AKT1
None
Datopotamab; Sacituzumab; Camizestrant
CTG-2768
Melanoma
BRAF
CDK4-high; CCND1-high
Vemurafenib; Palbociclib
CTG-2776
NSCLC
None
None
Palbociclib; Cis/Gem
CTG-3032
Gastric
BRCA2; PIK3CA
CDK4-high
Alpelisib
CTG-3063
Melanoma
BRAF
CDK4-high; CCND1-high; ERBB3-high
Vemurafenib; Palbociclib
CTG-3121
NSCLC
RB1
CDK4-high
Palbociclib; Trametinib; Avutometinib
CTG-3494
Colorectal
None
CCND1-high; MAPK3-high
Palbociclib; Trametinib; Avutometinib
CTG-3631
Colorectal
KRAS G12R
CDK4-high; ERBB3-high
Daraxonrasib; Sotorasib