| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 1.39M | 1.04M | 4.01M | 4.74M | 1.08M | 71.00K |
| Gross Profit | -149.00K | 1.04M | 4.01M | 3.35M | -184.00K | -56.93M |
| EBITDA | -420.58M | -338.85M | -221.51M | -166.90M | -106.78M | -72.59M |
| Net Income | -369.83M | -298.41M | -214.53M | -163.92M | -107.64M | -72.86M |
Balance Sheet | ||||||
| Total Assets | 1.29B | 1.43B | 635.35M | 352.18M | 351.01M | 183.44M |
| Cash, Cash Equivalents and Short-Term Investments | 1.20B | 1.35B | 558.55M | 334.43M | 333.71M | 170.88M |
| Total Debt | 49.94M | 51.72M | 51.73M | 3.08M | 3.07M | 4.01M |
| Total Liabilities | 118.05M | 109.79M | 96.25M | 35.85M | 19.07M | 14.53M |
| Stockholders Equity | 1.17B | 1.32B | 539.11M | 316.33M | 331.94M | 168.92M |
Cash Flow | ||||||
| Free Cash Flow | -307.80M | -229.81M | -171.00M | -116.86M | -89.02M | -62.21M |
| Operating Cash Flow | -301.80M | -225.97M | -166.31M | -115.20M | -88.59M | -62.03M |
| Investing Cash Flow | -569.49M | -574.82M | -200.41M | -173.98M | -56.48M | 217.00K |
| Financing Cash Flow | 622.86M | 1.01B | 388.94M | 121.96M | 252.68M | 114.57M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
64 Neutral | $3.73B | ― | -9.46% | ― | 40.54% | -264.26% | |
60 Neutral | $4.36B | ― | -31.14% | ― | ― | -11.39% | |
58 Neutral | $4.31B | ― | -32.09% | ― | -50.05% | -54.47% | |
55 Neutral | $4.00B | ― | -36.94% | ― | ― | -9.10% | |
52 Neutral | $2.52B | 66.39 | 14.10% | ― | 42.11% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $3.07B | ― | -325.76% | ― | 20.63% | 8.09% |
Crinetics Pharmaceuticals Inc. is conducting a Phase 1 study titled ‘A Phase 1, Randomized, Double-blind, Placebo-controlled Study to Assess Pharmacokinetics, Safety, and Tolerability of Atumelnant in Healthy Japanese and Caucasian Participants.’ The study aims to evaluate the pharmacokinetics, safety, and tolerability of the drug Atumelnant when administered in single and multiple doses to healthy volunteers from Japanese and Caucasian backgrounds. This research is significant as it explores the drug’s effects across different ethnic groups, potentially paving the way for broader applications.
Crinetics Pharmaceuticals is conducting a Phase 3 study titled ‘A Randomized, Parallel Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Paltusotine in Adults With Carcinoid Syndrome Due to Well-Differentiated Neuroendocrine Tumors.’ The study aims to assess the efficacy and safety of paltusotine, an oral treatment, in managing carcinoid syndrome, a condition associated with neuroendocrine tumors.
Crinetics Pharmaceuticals Inc. is conducting a Phase 1/2 study titled A Phase 1/2 Dose Escalation Study of CRN09682 With an Expansion Phase in Participants With Progressive Metastatic Somatostatin Receptor Type 2 (SST2)-Expressing Neuroendocrine Neoplasms (NENs) and Other SST2-Expressing Solid Tumors. The study aims to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of CRN09682, a drug targeting SST2-expressing tumors.
Crinetics Pharmaceuticals is conducting an extension study titled ‘An Open-label, Long-term Extension Study to Evaluate Safety and Efficacy in Participants Treated With CRN04894.’ The study aims to assess the long-term safety, tolerability, and efficacy of atumelnant (CRN04894) in treating Congenital Adrenal Hyperplasia, a significant condition affecting adrenal gland function.
Study Overview: Crinetics Pharmaceuticals is conducting a study titled ‘A Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Atumelnant in Adult Participants With Classic Congenital Adrenal Hyperplasia (Calm-CAH)’. The study aims to assess the safety and efficacy of Atumelnant in treating adults with classic congenital adrenal hyperplasia (CAH) due to 21-OHD, a condition that affects adrenal gland function.
Study Overview: Crinetics Pharmaceuticals is conducting a Phase 2/3 study titled A Phase 2/3 Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Atumelnant Treatment in Pediatric Participants With Congenital Adrenal Hyperplasia Including a Long-Term Extension. The study aims to assess the safety, efficacy, and pharmacokinetics of Atumelnant in children with congenital adrenal hyperplasia (CAH), a condition that affects hormone production. This research is significant as it addresses a critical need for effective treatments in pediatric endocrinology.
Crinetics Pharmaceuticals is conducting a study titled ‘A Phase 1b/2a Open-label Multiple-ascending Dose Exploratory Study of CRN04894 in ACTH-dependent Cushing’s Syndrome.’ This study aims to evaluate the safety, tolerability, and pharmacokinetics of CRN04894, an ACTH receptor antagonist, in treating Cushing’s Syndrome, a condition characterized by excessive cortisol production. The study’s significance lies in its potential to offer a new treatment avenue for patients with Cushing’s disease or Ectopic ACTH Syndrome.
On September 25, 2025, Crinetics Pharmaceuticals announced that the FDA approved PALSONIFYTM (paltusotine) for the first-line treatment of adults with acromegaly who had an inadequate response to surgery or for whom surgery is not an option. PALSONIFY, a once-daily oral therapy, marks a significant advancement in acromegaly treatment, offering a non-invasive alternative to traditional injections. The approval is based on successful Phase 3 trials demonstrating the drug’s efficacy and safety, and it represents a pivotal milestone for Crinetics as it enhances its position as a leader in endocrine-focused pharmaceuticals. The company is also working to ensure broad access to PALSONIFY and has launched a support program, CrinetiCARE, to assist patients throughout their treatment journey.
The most recent analyst rating on (CRNX) stock is a Buy with a $143.00 price target. To see the full list of analyst forecasts on Crinetics Pharmaceuticals stock, see the CRNX Stock Forecast page.
Crinetics Pharmaceuticals’ recent earnings call conveyed a mixed sentiment, highlighting both robust progress and looming challenges. The company demonstrated strong execution across its business, with notable advancements in its pipeline and financial stability. However, concerns were raised regarding high operational costs, cash usage, and potential hurdles in launching PALSONIFY.
Crinetics Pharmaceuticals is a clinical-stage pharmaceutical company specializing in the discovery, development, and commercialization of novel therapeutics for endocrine diseases and endocrine-related tumors. The company’s lead development candidate, PALSONIFY (paltusotine), is in clinical development for acromegaly and carcinoid syndrome associated with neuroendocrine tumors.