- |||||||||| Perjeta (pertuzumab) / Roche
Incidence of hypomagnesemia in patients with HER2+ breast cancer treated with pertuzumab. () - Apr 26, 2023 - Abstract #ASCO2023ASCO_4182; Our results do not indicate clinical monitoring of hypomagnesemia is necessary for patients receiving P. >* The values were converted into categorical variables (Y/N), since both institutions had different lab reference values.**4th trial date unavailable for 2 patients. One patient received only 3 cycles of P; one patient transferred care elsewhere after 3 cycles of P.
- |||||||||| Erbitux (cetuximab) / Eli Lilly, EMD Serono, Braftovi (encorafenib) / Ono Pharma, Pierre Fabre, Pfizer
BREAKWATER: An open-label, multicenter, randomized, phase 3 study, with a safety lead-in (SLI), of first-line (1L) encorafenib (E) + cetuximab (C) (Available On Demand; Poster Bd # 325b) - Apr 26, 2023 - Abstract #ASCO2023ASCO_3145; P3 bCohort 3 to begin after phase 3 enrollment is complete. cBy BICR.BICR, blinded independent central review; CAPOX, capecitabine/oxaliplatin; FOLFIRI, fluorouracil/leucovorin/irinotecan; FOLFOX, fluorouracil/leucovorin/oxaliplatin; FOLFOXIRI, fluorouracil/leucovorin/oxaliplatin/irinotecan.
- |||||||||| Erbitux (cetuximab) / Eli Lilly, EMD Serono
Analysis of primary and acquired resistance to cetuximab from multiomic data in the New EPOC trial. (On Demand | Hall A; Poster Bd # 277) - Apr 26, 2023 - Abstract #ASCO2023ASCO_3095; After neoadjuvant treatment, gain/amplification of MET was associated with a shorter survival with ChemoCetux. By contrast MAPK pathway mutations were largely unchanged supporting earlier findings that alternative resistance mechanisms predominate when EGFRi is combined with chemotherapy.
- |||||||||| Erbitux (cetuximab) / Eli Lilly, EMD Serono, ASN007 / Asana BioSci, Erasca, UT MD Anderson Cancer Center, Braftovi (encorafenib) / Ono Pharma, Pierre Fabre, Pfizer
Preliminary results from ERAS-007 plus encorafenib and cetuximab (EC) in patients (pts) with metastatic BRAF V600E mutated colorectal cancer (CRC) in HERKULES-3 study: A phase 1b/2 study of agents targeting the mitogen-activated protein kinase (MAPK) pathway in pts with advanced gastrointestinal malignancies (GI cancers). (On Demand | Hall A; Poster Bd # 257) - Apr 26, 2023 - Abstract #ASCO2023ASCO_3076; P1b/2 The highest dose of ERAS-007 evaluated and cleared by the safety review committee to date is 100 mg BID-QW when combined with EC. Observed PK, toxicity, and preliminary activity support continued evaluation of this combination in pts with BRAF V600E CRC.
- |||||||||| garsorasib (D-1553) / InventisBio
Trial completion date, Trial primary completion date, Metastases: KEYNOTE-C15: Study to Evaluate D-1553 in Subjects With Solid Tumors (clinicaltrials.gov) - Apr 25, 2023 P1/2, N=200, Recruiting, Trial completion date: Apr 2025 --> Feb 2027 | Trial primary completion date: Apr 2025 --> Feb 2027 Trial completion date: Feb 2023 --> Feb 2025 | Trial primary completion date: Nov 2022 --> Nov 2024
- |||||||||| Erbitux (cetuximab) / Eli Lilly, EMD Serono
Enrollment open, Combination therapy: Pilot Study of Imatinib Cetuximab Combo for H & N Cancer (clinicaltrials.gov) - Apr 25, 2023 P1, N=15, Recruiting, Trial completion date: Feb 2023 --> Feb 2025 | Trial primary completion date: Nov 2022 --> Nov 2024 Not yet recruiting --> Recruiting
|