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Celcuity/$CELC

1D1W1M3M6MYTD1Y5YMAX

About Celcuity

Celcuity Inc is a clinical-stage biotechnology company developing targeted therapies for multiple solid tumors. Its candidate, gedatolisib, is a kinase inhibitor of the PI3K/AKT/mTOR (PAM) pathway, binding all class I PI3K isoforms and mTORC1/2, offering comprehensive inhibition with a mechanism and pharmacokinetics differentiated from other therapies. The Phase 3 VIKTORIA-1 trial, evaluating gedatolisib with fulvestrant, with or without palbociclib, in HR+/HER2- breast cancer, has completed enrollment and reported results for PIK3CA WT tumors, with cohort 2 (PIK3CA MT) also enrolled. Phase 3 VIKTORIA-2 and Phase 1b/2 CELC-G-201 trials, evaluating combinations in endocrine-resistant HR+/HER2- breast cancer and metastatic castration-resistant prostate cancer, are ongoing.
Ticker
$CELC
Sector
Health
Primary listing
NASDAQ
Employees
155

Celcuity Metrics

BasicAdvanced
$3.2B
-
-$4.72
0.13
-

What the Analysts think about Celcuity

Analyst ratings (Buy, Hold, Sell) for Celcuity stock.
Analyst projections of the future price of Celcuity stock.

Bulls say / Bears say

FDA approval and the September commercial launch give Celcuity its first marketed product and a route to revenue in second-line HR+/HER2− breast cancer. REVTORPYK is approved for patients without a detected PIK3CA mutation. (Reuters, Celcuity)
Phase 3 results support a possible label expansion to PIK3CA-mutated disease: the triplet cut progression or death risk by half versus alpelisib plus fulvestrant, and the FDA has accepted Celcuity’s supplemental application with a June 2027 decision date. (Celcuity, Celcuity)
Early launch indicators suggest broad access: 78% of Celcuity’s top 36 strategic accounts had ordered the drug, while health plans covering 91% of US commercial and Medicare lives included it. REVTORPYK also gained a preferred Category 1 NCCN recommendation for the approved setting. (Celcuity)
The PIK3CA-mutant Phase 3 results fell short of some investors’ expectations: median progression-free survival was about 11 months, below the 14.6-month result in an earlier, much smaller study. The triplet also did not clearly outperform the doublet, leaving uncertainty over which regimen doctors will favour. (BioPharma Dive)
The triplet’s efficacy comes with a substantial treatment burden: reported Grade 3 or higher neutropenia affected 62.3% of patients and stomatitis 19.2%, and two treatment-related deaths occurred in the triplet group. These risks could complicate prescribing and patient management. (Medscape)
Celcuity’s cash burn and debt raise the execution stakes: it used $66.2 million of operating cash in the third quarter and reported a $73.3 million loss, while carrying about $754 million in convertible notes. Continued commercial and trial spending will need to translate into revenue to limit future financing or dilution risk. (Celcuity, SEC)
Data summarised monthly by Lightyear AI. Last updated on 12 Nov 2026.

Celcuity Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Celcuity Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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