Celcuity Inc.

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Sep. 09	Celcuity Inc. Presents at Citigroup?s Biopharma Back to School Summit 2026, Sep-09-2026 08:00 AM
Aug. 26	Celcuity Inc Submits Supplemental New Drug Application to Fda for Revtorpyk (Gedatolisib) for Hr+/Her2-, Pik3ca Mutant Locally Advanced or Metastatic Breast Cancer	CI

Published on 07/15/2026 at 04:57 pm EDT - Modified on 07/16/2026 at 07:30 am EDT

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Presentation Operator Message
Operator (Operator)

Hello, and welcome to Celcuity conference call. [Operator Instructions]

I would now like to hand the conference over to

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Sep. 09	Celcuity Inc. Presents at Citigroup?s Biopharma Back to School Summit 2026, Sep-09-2026 08:00 AM
Aug. 26	Celcuity Inc Submits Supplemental New Drug Application to Fda for Revtorpyk (Gedatolisib) for Hr+/Her2-, Pik3ca Mutant Locally Advanced or Metastatic Breast Cancer	CI
Aug. 26	Celcuity Submits Supplemental NDA for REVTORPYK in PIK3CA-Mutant Breast Cancer	MT
Aug. 13	Celcuity Inc., Q2 2026 Earnings Call, Aug 13, 2026
Aug. 13	Celcuity Q2 Adjusted Loss Widens	MT
Aug. 13	Earnings Flash (CELC) Celcuity Inc. Posts Q2 Adjusted Loss $1.07 per Share, vs. FactSet Est of $-1.12	MT
Aug. 13	Celcuity Inc. Reports Earnings Results for the Second Quarter and Six Months Ended June 30, 2026	CI
Jul. 30	Celcuity Announces FDA Approval And NCCN Guidelines Inclusion For REVTORPYK In Combination With Fulvestrant With Or Without Palbociclib	CI
Jul. 15	Celcuity Inc. - Special Call
Jul. 15	Celcuity shares fall as launch delay eclipses US approval for breast cancer drug	RE
Jul. 15	Celcuity shares fall as delayed breast cancer drug launch eclipses first US FDA approval	RE
Jul. 14	Celcuity Gets FDA Approval for Breast Cancer Drug	DJ
Jul. 14	Celcuity's REVTORPYK Gets FDA Approval for HR+/HER2- Breast Cancer	MT
Jul. 14	Celcuity Announces FDA Approval of REVTORPYK? (Gedatolisib) for the Treatment of HR+/HER2-, PIK3CA Wild-Type Locally Advanced or Metastatic Breast Cancer	CI
Jul. 14	Correction to Celcuity Gets FDA Approval Headline	DJ

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