Drug intelligence / Profile preview

dabrafenib + panitumumab

Development stage
Unknown
Lead developer
GSK
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

dabrafenib + panitumumab is an investigational combination therapy studied for the treatment of metastatic colorectal cancer (CRC) with the BRAF V600E mutation. Dabrafenib is a small molecule inhibitor targeting BRAF V600E, which blocks downstream signaling in the MAPK pathway, thereby inhibiting cancer cell proliferation. Panitumumab is a monoclonal antibody targeting the extracellular domain of the epidermal growth factor receptor (EGFR), blocking ligand-induced activation and subsequent signaling. Together, the combination aims to overcome adaptive resistance mechanisms—specifically, feedback reactivation of MAPK signaling through EGFR—seen with BRAF inhibitor monotherapy in CRC[1][4][6]. Clinical trials tested full monotherapy doses (dabrafenib 150 mg orally twice daily and panitumumab 6 mg/kg IV every 2 weeks) and showed manageable safety with common toxicities including mild-moderate dermatitis acneiform, nausea, fatigue, and diarrhea[1][6]. Confirmed objective response rate was 10% in heavily pre-treated patient cohorts[4][6].

Brand names
Tafinlar (dabrafenib)Vectibix (panitumumab)
Other names
dabrafenib + panitumumab
02

Targets

BRAF V600EEGFR T790M (Epidermal growth factor receptor T790M mutant)

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