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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Effect of Tusamitamab Ravtansine on QTc Interval in Participants With Metastatic Solid Tumors

Excerpt:
...- Expression of carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) will be assessed centrally using the most recent archival tumor tissue (or, if...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

INTRUSION: Unraveling the INTRatUmoral PK/PD relatION for SAR408701

Excerpt:
...Intratumoral tusamitamab ravtansine concentration`Incidence of grade 3 or 4 adverse events`Response to treatment`CEACAM5 expression`RNA expression levels`circulating CEA levels`tumor genomic features`Maximal plasma concentration`AUCinf`AUClast`AUCt`Thalf`systemic tusamitamab ravtansine concentration`Volume of distribution`concentration DM4 metabolites: Lys-SPDB-DM4, Me-Dm4`features in tumor micro-environment...
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Evaluation of SAR408701 in Patients With Advanced Solid Tumors

Excerpt:
...Patient must consent to a baseline biopsy for retrospective confirmation of tumor CEACAM5 expression, except if NSCLC or SCLC without lesion amenable to biopsy....
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: D – Preclinical
Source:
Title:

Abstract 4151: Anti-CEACAM5 immune stimulant TLR7/8 agonist antibody drug conjugate is a potent myeloid cell activator for the treatment of CEACAM5-expressing tumors

Published date:
04/04/2023
Excerpt:
In co-culture of human blood cells and human CEACAM5+ gastric cancer cells, it was shown to induce phagocytosis activity, associated with increased activation/maturation of both monocytes and dendritic cells. Tusamitamab R848 ADC evaluated in vivo in CEACAM5+ pancreatic human tumor model, HPAFII, leads to robust antitumor activity with complete regressions (CR) after single administration at 5 mg/kg....Based on preclinical in vitro and in vivo data, the tusamitamab R848 ADC is an innovative ADC approach with the potential to eradicate CEACAM5+ tumors in patients.
DOI:
https://doi.org/10.1158/1538-7445.AM2023-4151