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A Study of the Safety and Tolerability of ABBV-621 in Participants With Previously-Treated Solid Tumors and Hematologic Malignancies

ABSTRACT: This is an open-label, Phase I, dose-escalation study to determine the maximum tolerated dose (MTD) and/or recommended phase two dose (RPTD), and evaluate the safety, efficacy, and pharmacokinetic (PK) profile of ABBV-621 for participants with previously-treated solid tumors or hematologic malignancies. Only chemotherapy combination (ABBV-621 + FOLFIRI) enrolling participants with RAS-mutant CRC who have received one prior line of therapy is open for enrollment.

DISEASE(S): Hematologic Neoplasms,Hematologic Malignancies,Advanced Solid Tumors,Solid Tumors,Neoplasms,Cancer

PROVIDER: 2238930 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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