REVTORPYK (gedatolisib) + fulvestrant, with or without palbociclib

HR-positive, HER2-negative, PIK3CA wild-type advanced breast cancer · Adults with HR-positive, HER2-negative locally advanced or metastatic breast cancer without a detected PIK3CA mutation after progression on or after at least one endocrine-therapy line in the metastatic setting

CELC · Celcuity

監管認定

完整時間線

6 個里程碑

FDA approved REVTORPYK regimens

FDA approved REVTORPYK with fulvestrant, with or without palbociclib, for the specified HR-positive, HER2-negative, PIK3CA wild-type locally advanced or metastatic breast cancer population. The approval came three days before the July 17 PDUFA date.

FDA — REVTORPYK approval

VIKTORIA-1 results were published

The PIK3CA wild-type cohort results were published in the Journal of Clinical Oncology. The triplet and doublet reduced the risk of progression or death by 76% and 67%, respectively, versus fulvestrant.

Celcuity — Publication of VIKTORIA-1 results

FDA accepted the NDA with Priority Review

FDA accepted the gedatolisib NDA, granted Priority Review and assigned a July 17, 2026 PDUFA goal date. The application was submitted under the Real-Time Oncology Review program.

Celcuity — NDA acceptance and Priority Review

Updated VIKTORIA-1 results were presented

Celcuity presented updated efficacy and safety findings from the PIK3CA wild-type cohort at the 2025 San Antonio Breast Cancer Symposium.

Celcuity — Updated VIKTORIA-1 results

相關新聞

資訊僅供研究 · 日期可能發生變化 · 最後更新 2026年8月13日