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DRUG:

mavelertinib (PF-06747775)

i
Other names: PFE-X775, PF-7775, PF-06747775, PF06747775, PF 06747775, PF6747775, PF 6747775, PF-6747775
Associations
Trials
Company:
Pfizer
Drug class:
EGFR inhibitor
Related drugs:
Associations
Trials
over2years
A phase 1b/2 study of PF-06747775 as monotherapy or in combination with Palbociclib in patients with epidermal growth factor receptor mutant advanced non-small cell lung cancer. (PubMed, Expert Opin Investig Drugs)
Median progression-free survival (90% CI) was 8.1 (5.4-23.3) months. PF-06747775 had a manageable safety profile and the study design highlights important considerations for future anti-EGFR agent development.
P1/2 data • Clinical Trial,Phase II • Journal • Combination therapy
|
EGFR (Epidermal growth factor receptor)
|
EGFR mutation
|
Ibrance (palbociclib) • mavelertinib (PF-06747775)
over3years
Study For Patients With NSCLC EGFR Mutations (Del 19 or L858R +/- T790M) (clinicaltrials.gov)
P1/2, N=65, Terminated, Pfizer | Phase classification: P2 --> P1/2
Clinical • Phase classification
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR mutation • EGFR L858R • EGFR exon 19 deletion • EGFR T790M
|
Ibrance (palbociclib) • Bavencio (avelumab) • mavelertinib (PF-06747775)
almost4years
Complex Crystal Structures of EGFR with Third-Generation Kinase Inhibitors and Simultaneously Bound Allosteric Ligands. (PubMed, ACS Med Chem Lett)
Here, we present the first complex crystal structures of mutant EGFR in complex with third-generation inhibitors such as osimertinib and mavelertinib in the presence of simultaneously bound allosteric inhibitors. These structures highlight the possibility of further combinations targeting EGFR and lay the foundation for hybrid inhibitors as next-generation TKIs.
Journal
|
EGFR (Epidermal growth factor receptor)
|
EGFR mutation • EGFR T790M • EGFR C797S
|
Tagrisso (osimertinib) • mavelertinib (PF-06747775)
4years
Study For Patients With NSCLC EGFR Mutations (Del 19 or L858R +/- T790M) (clinicaltrials.gov)
P2; N=65; Terminated; Sponsor: Pfizer; Completed --> Terminated; The study was ended for strategic reasons and changes in the external environment. The safety profile and risk benefit ratio for PF-0674775 remained unchanged.
Trial termination • Clinical
|
EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
|
EGFR mutation • EGFR L858R • EGFR exon 19 deletion • EGFR T790M
|
Oncomine™ Dx Target Test
|
Ibrance (palbociclib) • Bavencio (avelumab) • mavelertinib (PF-06747775)