Market Cap 4.68B
Revenue (ttm) 761.41M
Net Income (ttm) 99.65M
EPS (ttm) N/A
PE Ratio 53.54
Forward PE 186.81
Profit Margin 13.09%
Debt to Equity Ratio 0.00
Volume 1,734,900
Avg Vol 1,783,552
Day's Range N/A - N/A
Shares Out 106.37M
Stochastic %K 94%
Beta 0.25
Analysts Sell
Price Target $67.40

Company Profile

Corcept Therapeutics Incorporated, a biopharmaceutical company, engages in the discovery and development of medications to treat severe endocrinologic, oncologic, metabolic, and neurologic disorders in the United States. The company offers Korlym, an oral medication for the treatment of hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing's syndrome who have type 2 diabetes mellitus or glucose intolerance and have failed surgery or are not candidates for surgery....

Industry: Biotechnology
Sector: Healthcare
Phone: 650 327 3270
Address:
101 Redwood Shores Parkway, Redwood City, United States
aristocks
aristocks Apr. 18 at 10:23 PM
$CORT so far so good!
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Orbit100
Orbit100 Apr. 17 at 4:23 PM
$CORT The approval represents a reversal for relacorilant in oncology following a CRL and 2021 decision to halt phase 3 trials in pancreatic cancer, where the benefit fell short of justifying further study. The company has nevertheless kept a foothold in pancreatic cancer, continuing to test relacorilant in the phase 2 Trident trial, while also advancing its development in endometrial cancer.
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Orbit100
Orbit100 Apr. 17 at 4:23 PM
$CORT Corcept Therapeutics has pulled off a significant turnaround for its once-troubled glucocorticoid receptor antagonist relacorilant, winning approval in ovarian cancer and sidestepping the toxicity concerns that derailed this drug in Cushing's syndrome. Now branded Lifyorli, relacorilant secured US approval months before its July PDUFA date, backed by survival data from the pivotal Rosella trial, which most recently showed that adding the drug to Abraxane cut the risk of death by 35%. The green light is particularly notable given relacorilant's history: in Cushing's syndrome Corcept was handed a complete response letter after regulators flagged a risk of drug-induced liver injury. This time, however, those concerns appear to have faded, with no liver-related adverse events reported in the Rosella trial at last year's ASCO; the label carries no boxed warning for hepatotoxicity.
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Orbit100
Orbit100 Apr. 17 at 4:22 PM
$CORT Korlym (Mifepristone): The company’s FDA-approved, flagship drug for controlling hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome. ir.corcept.com ir.corcept.com +5 Corcept holds over 30 clinical-stage compounds, maintaining a focus on cortisol regulation to treat severe diseases. The company continues to see strong sales growth for Korlym.
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Orbit100
Orbit100 Apr. 17 at 4:22 PM
$CORT Key Pipeline Assets & Status (As of April 2026): Relacorilant (Cushing’s & Oncology): Ovarian Cancer: FDA-approved (March 2026) in combination with nab-paclitaxel for platinum-resistant ovarian, fallopian tube, or primary peritoneal cancer. Cushing’s Syndrome: Phase 3 GRACE trial met its primary endpoint, showing positive results for reducing hypercortisolism. A new drug application (NDA) is being prepared following discussions with the FDA. Other Solid Tumors: Being studied in endometrial, cervical, pancreatic, and prostate cancers. Dazucorilant: Currently under evaluation for Amyotrophic Lateral Sclerosis (ALS) and solid tumors, with studies completed regarding its pharmacokinetics and safety profile. Miricorilant: Investigated for the treatment of Non-Alcoholic Steatohepatitis (NASH) and to mitigate antipsychotic-induced weight gain. Korlym (Mifepristone): The company’s FDA-approved, flagship drug for controlling hyperglycemia secondary to hypercortisolism in adult patients
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Orbit100
Orbit100 Apr. 17 at 4:20 PM
$CORT Stay the course. The core business of the company is still good with 4 drugs in its pipe line. Corcept Therapeutics (NASDAQ:CORT) is advancing a strong pipeline of selective cortisol modulators, with relacorilant leading in both Cushing's syndrome (Phase 3 GRACE trial) and oncology (FDA-approved with nab-paclitaxel for ovarian cancer). Other key compounds include dazucorilant (ALS, solid tumors) and miricorilant (NASH, antipsychotic-induced weight gain), targeting broad endocrinology, oncology, and neurology markets.
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gucag006
gucag006 Apr. 14 at 8:02 PM
$CORT Q1 ER on 5/5/2026 after Market Close.
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Orbit100
Orbit100 Apr. 14 at 6:28 PM
$CORT Be patient. Corcept will have 50 to 60% more room to go and you will see over $65 eventually. Be strong. Watch pot doesn't boil.
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gucag006
gucag006 Apr. 14 at 6:27 AM
$CORT From Gemini AI Pro, the global market potential for Lifyorli:
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Orbit100
Orbit100 Apr. 13 at 6:40 PM
$CORT Stay tune for 50 to 60% upside minimum for Corcept. Look at RVMD for the news of its drug proven survival rate for pancreatic cancer. Corcept will have its day, mark my post.
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Latest News on CORT
Corcept Therapeutics Stock Plunges As Court Clears Teva Generic

Feb 19, 2026, 11:48 AM EST - 2 months ago

Corcept Therapeutics Stock Plunges As Court Clears Teva Generic


Corcept's cancer drug meets main goal in late-stage trial

Jan 22, 2026, 8:13 AM EST - 3 months ago

Corcept's cancer drug meets main goal in late-stage trial


aristocks
aristocks Apr. 18 at 10:23 PM
$CORT so far so good!
0 · Reply
Orbit100
Orbit100 Apr. 17 at 4:23 PM
$CORT The approval represents a reversal for relacorilant in oncology following a CRL and 2021 decision to halt phase 3 trials in pancreatic cancer, where the benefit fell short of justifying further study. The company has nevertheless kept a foothold in pancreatic cancer, continuing to test relacorilant in the phase 2 Trident trial, while also advancing its development in endometrial cancer.
0 · Reply
Orbit100
Orbit100 Apr. 17 at 4:23 PM
$CORT Corcept Therapeutics has pulled off a significant turnaround for its once-troubled glucocorticoid receptor antagonist relacorilant, winning approval in ovarian cancer and sidestepping the toxicity concerns that derailed this drug in Cushing's syndrome. Now branded Lifyorli, relacorilant secured US approval months before its July PDUFA date, backed by survival data from the pivotal Rosella trial, which most recently showed that adding the drug to Abraxane cut the risk of death by 35%. The green light is particularly notable given relacorilant's history: in Cushing's syndrome Corcept was handed a complete response letter after regulators flagged a risk of drug-induced liver injury. This time, however, those concerns appear to have faded, with no liver-related adverse events reported in the Rosella trial at last year's ASCO; the label carries no boxed warning for hepatotoxicity.
0 · Reply
Orbit100
Orbit100 Apr. 17 at 4:22 PM
$CORT Korlym (Mifepristone): The company’s FDA-approved, flagship drug for controlling hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome. ir.corcept.com ir.corcept.com +5 Corcept holds over 30 clinical-stage compounds, maintaining a focus on cortisol regulation to treat severe diseases. The company continues to see strong sales growth for Korlym.
0 · Reply
Orbit100
Orbit100 Apr. 17 at 4:22 PM
$CORT Key Pipeline Assets & Status (As of April 2026): Relacorilant (Cushing’s & Oncology): Ovarian Cancer: FDA-approved (March 2026) in combination with nab-paclitaxel for platinum-resistant ovarian, fallopian tube, or primary peritoneal cancer. Cushing’s Syndrome: Phase 3 GRACE trial met its primary endpoint, showing positive results for reducing hypercortisolism. A new drug application (NDA) is being prepared following discussions with the FDA. Other Solid Tumors: Being studied in endometrial, cervical, pancreatic, and prostate cancers. Dazucorilant: Currently under evaluation for Amyotrophic Lateral Sclerosis (ALS) and solid tumors, with studies completed regarding its pharmacokinetics and safety profile. Miricorilant: Investigated for the treatment of Non-Alcoholic Steatohepatitis (NASH) and to mitigate antipsychotic-induced weight gain. Korlym (Mifepristone): The company’s FDA-approved, flagship drug for controlling hyperglycemia secondary to hypercortisolism in adult patients
0 · Reply
Orbit100
Orbit100 Apr. 17 at 4:20 PM
$CORT Stay the course. The core business of the company is still good with 4 drugs in its pipe line. Corcept Therapeutics (NASDAQ:CORT) is advancing a strong pipeline of selective cortisol modulators, with relacorilant leading in both Cushing's syndrome (Phase 3 GRACE trial) and oncology (FDA-approved with nab-paclitaxel for ovarian cancer). Other key compounds include dazucorilant (ALS, solid tumors) and miricorilant (NASH, antipsychotic-induced weight gain), targeting broad endocrinology, oncology, and neurology markets.
0 · Reply
gucag006
gucag006 Apr. 14 at 8:02 PM
$CORT Q1 ER on 5/5/2026 after Market Close.
0 · Reply
Orbit100
Orbit100 Apr. 14 at 6:28 PM
$CORT Be patient. Corcept will have 50 to 60% more room to go and you will see over $65 eventually. Be strong. Watch pot doesn't boil.
0 · Reply
gucag006
gucag006 Apr. 14 at 6:27 AM
$CORT From Gemini AI Pro, the global market potential for Lifyorli:
0 · Reply
Orbit100
Orbit100 Apr. 13 at 6:40 PM
$CORT Stay tune for 50 to 60% upside minimum for Corcept. Look at RVMD for the news of its drug proven survival rate for pancreatic cancer. Corcept will have its day, mark my post.
0 · Reply
Night_Owl_Biotech
Night_Owl_Biotech Apr. 12 at 2:42 PM
Commercial-stage oncology focused bio 5 year revenue multiples v. DAWN. All market caps are per Yahoo Finance so DAWN valuations do not consider fully diluted shares, consistent with peers. We provide DAWN revenue multiples using analyst consensus, again consistent with DAWN's peers, and per DAWN mgmt/BOD. $SNDX trades @ 0.61X 5-year analyst consensus. DAWN trades for 1.03X the same 5-year analyst consensus. Hence, if SNDX were acquired at the same 5-year multiple as DAWN, SNDX would trade @ 1.03X 5 year consensus. This is roughly 70% higher than where SNDX trades today. SNDX revenues generated 96% gross margins in FY25 where DAWN's like margins were 89%. Does this mean SNDX should command a proportionally higher multiple? We'd otherwise caution investors to expect peers on the attachment with smaller market caps to expect DAWN like M&A multiples. $CORT updated analyst consensus are roughly 10% lower than per the attachment This is not investment advice. $JAZZ $IOVA $NUVB
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Orbit100
Orbit100 Apr. 11 at 6:43 PM
$CORT I am a big believer that Corcept still have 50% to 60% of a rally ahead of them. Stay tune.
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jsmith5788
jsmith5788 Apr. 10 at 8:53 PM
$CORT https://ir.corcept.com/news-releases/news-release-details/corcept-presents-complete-data-pivotal-rosella-trial-sgo-late
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Quantumup
Quantumup Apr. 10 at 4:55 PM
UBS⬆️ $AXSM's PT to $259 from $251 and reiterated a Buy rating. $CORT $DNLI BMY OTSKY UBS said in its note: AXSM is a rarefied CNS growth platform that can get a premium standalone multiple in a M&A-rich biotech tape. With the April 30th PDUFA date for Auvelity's ADA filing approaching, investor focus is on the potential label and what initial launch dynamics could look like if approved. Notably, given the recent patterns of the FDA issuing approval decisions ahead of formal PDUFA dates (e.g. Corcept's relacorilant, Denali's tividenofusp alfa), a decision could come earlier. We have high conviction in Auvelity's approvability in ADA, and believe the new indication could add ~$2BN in incremental sales. We update our model to reflect BS/CF actuals, leading to a revised PT of $259 (from $251).
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StocktwitsNews
StocktwitsNews Apr. 10 at 4:27 PM
This Small-Cap Biotech Stock Just Hit A Near 22-Month High – But This Analyst Still Expects Another 56% Rally $ZNTL $CORT https://stocktwits.com/news/equity/markets/sntl-stock-rally-ovarian-cancer-trial-update/cZJ0S9XRItq
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JamesThomasRice
JamesThomasRice Apr. 9 at 1:45 PM
$CORT tick tock. This can really get going when that eod bidwhacker finishes up
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mrgorbachev
mrgorbachev Apr. 8 at 6:29 PM
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gucag006
gucag006 Apr. 8 at 1:44 AM
$CORT Deep Dive into Dazucorilant for ALS - Part 2 Phase 2 Trial Results: - Missed its primary goal regarding disease progression but showed a marked improvement in survival. - Primary Endpoint: There was no statistically significant difference in the decline of ALS Functional Rating Scale-Revised (ALSFRS-R) scores between the patients taking dazucorilant and placebo over the 24-week period. - Secondary Endpoint: Met its secondary endpoint by demonstrating a statistically significant extension in overall survival. - 24-Week Data: At the end of the initial 6-month double-blind period, there were zero deaths among the 83 patients receiving the 300 mg dose, compared to 5 deaths in (82) placebo group. - June 2025 Update: Patients with 300 mg dose showed a significantly lower risk of death compared to patients who were originally on the placebo and did not enter the extension phase. CORT is in discussions with FDA and EMA to determine the necessary next steps for advancing the drug.
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gucag006
gucag006 Apr. 8 at 1:33 AM
$CORT Deep Dive into Dazucorilant for ALS - Part 1 How does it work: - Chronically elevated cortisol levels can cause neuroinflammation and nerve cell damage. - Patients with rapid ALS progression often exhibit these elevated cortisol levels. By blocking the glucocorticoid receptor, dazucorilant aims to mitigate these neurotoxic effects. Phase 2 (NCT05407324) Trial DAZALS : - A double-blind, placebo-controlled trial with 249 adults with ALS across North America and Europe. - Treatment Arms: Patients were randomized (1:1:1) to receive either 150 mg of dazucorilant, 300 mg of dazucorilant, or a placebo once daily. - Timeline: The test lasted 24 weeks, followed by an open-label extension (OLE) allowing all eligible participants to receive the 300 mg dose of dazucorilant for an extended period.
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gucag006
gucag006 Apr. 7 at 9:07 PM
$CORT Deep dive into Miricorilant for NASH/MASH - Part 2 Phase 2b MONARCH trial (on going): - Dosing Breakthrough: Intermittently (twice a week) instead of daily does provided a gradual, safe reduction in liver fat (around 30% over 12 weeks) without elevating liver enzymes. - Status: 175 adult patients with confirmed NASH/MASH and liver fibrosis receive either a placebo or 100 mg of Miricorilant twice a week for up to 48 weeks. - The Goals: The trial is looking to officially confirm that this twice-a-week dosing effectively reduces liver fat, resolves liver inflammation, and improves fibrosis scarring over the long term. - Timeline: Primary completion estimated for late 2026. If successful, it will pave the way for massive Phase 3 trials in 2027 and possible NDA and FDA approval in 2028. TAM: - Currently estimated between $3B and $7.9B. - Projected to skyrocket from $24B to over $31.8B by 2033. Competitive Landscape: Rezdiffra (resmetirom) approved in 2024 & Wegovy (semaglutide) label expansion.
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gucag006
gucag006 Apr. 7 at 8:44 PM
$CORT Deep dive into Miricorilant for NASH/MASH - Part 1 How does it work: - Cortisol plays a massive role in regulating your metabolism, heightened cortisol activity in the liver drives the accumulation of liver fat, insulin resistance, and inflammation. - Cortisol binds to specific receptors in the body (GR, MR), and Miricorilant acts as a targeted blocker/modulator for these specific receptors. By blocking excess cortisol activity in the liver, Miricorilant helps remodel the way the liver processes lipids (fats), which leads to a rapid reduction in liver fat buildup (steatosis) and helps improve broader metabolic issues like high triglycerides and insulin resistance. Phase 1 & 2a Results: - Patients on Miricorilant saw massive relative reductions in liver fat—ranging from 38% to nearly 74% reduction in just 4 to 6 weeks rarely seen with other drugs, which also caused severe but temporary spikes in liver enzymes (ALT and AST). Because of this safety concern, the trial had to be halted.
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Johnnytwofour2
Johnnytwofour2 Apr. 7 at 4:27 PM
$CORT Nice recovery from yesterday's closing dump.
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