Drug intelligence / Profile preview

FWD1802 + ribociclib

Development stage
Phase 2
Lead developer
Shenzhen Forward Pharmaceutical
Modality
Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Molecules
Administration
Oral
01

Overview

Fwd1802 + ribociclib is an investigational combination therapy for estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, unresectable locally advanced or metastatic breast cancer. FWD1802 is a third-generation, oral selective estrogen receptor degrader (SERD) that binds the estrogen receptor (ER) competitively with higher affinity than fulvestrant, aiming to degrade ER and overcome resistance from ESR1 mutations. Ribociclib is an approved, oral small molecule inhibitor of cyclin-dependent kinases 4 and 6 (CDK4/6), designed to suppress cell cycle progression. The combination is being evaluated to maximize anti-tumor activity due to their complementary mechanisms in ER+/HER2- breast cancer, especially for patients who have progressed on previous endocrine therapy.

02

Targets

CDK4 (Cyclin-dependent kinase 4)CDK6 (Cyclin-dependent kinase 6)ER (Estrogen receptor)

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