| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 2.68B | 2.36B | 1.89B | 1.49B | 1.13B | 1.05B |
| Gross Profit | 2.64B | 2.32B | 1.85B | 1.47B | 1.12B | 1.04B |
| EBITDA | 665.40M | 639.70M | 416.10M | 264.60M | 138.10M | 148.10M |
| Net Income | 428.00M | 341.30M | 249.70M | 154.50M | 89.60M | 407.30M |
Balance Sheet | ||||||
| Total Assets | 4.27B | 3.72B | 3.25B | 2.37B | 2.07B | 1.73B |
| Cash, Cash Equivalents and Short-Term Investments | 1.11B | 1.08B | 1.03B | 989.30M | 711.30M | 801.00M |
| Total Debt | 428.40M | 455.10M | 428.40M | 262.90M | 440.40M | 412.30M |
| Total Liabilities | 1.26B | 1.13B | 1.02B | 660.90M | 698.50M | 608.50M |
| Stockholders Equity | 3.00B | 2.59B | 2.23B | 1.71B | 1.37B | 1.13B |
Cash Flow | ||||||
| Free Cash Flow | 593.10M | 557.20M | 361.60M | 322.90M | 233.10M | 217.60M |
| Operating Cash Flow | 636.80M | 595.40M | 389.90M | 339.40M | 256.50M | 228.50M |
| Investing Cash Flow | -279.80M | -126.80M | -467.10M | -177.10M | -130.20M | 4.10M |
| Financing Cash Flow | -365.60M | -486.70M | 65.30M | -234.30M | 27.40M | -157.80M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
79 Outperform | $15.19B | 36.39 | 14.96% | ― | 19.61% | 11.36% | |
74 Outperform | $1.10B | 10.65 | 14.84% | ― | -0.03% | -27.66% | |
67 Neutral | $11.34B | 16.47 | 17.72% | 0.68% | 10.63% | 6.35% | |
63 Neutral | $27.94B | 39.15 | 10.81% | ― | -0.25% | ― | |
55 Neutral | $11.66B | ― | -21.09% | 4.58% | -6.40% | -320.23% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $981.78M | ― | 2.90% | ― | 3.14% | ― |
Neurocrine Biosciences’ recent earnings call painted a picture of robust growth and strategic foresight. The company reported a strong quarter, marked by significant revenue growth and successful commercial performance of its key products, CRENESSITY and INGREZZA. Despite facing challenges such as the Inflation Reduction Act and a Department of Justice investigation, Neurocrine is proactively expanding its sales force and advancing its clinical pipeline, positioning itself for sustained future growth.
Neurocrine Biosciences has recently completed a Phase 2 clinical study titled ‘A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of NBI-1070770 in Adults With Major Depressive Disorder.’ The study aimed to evaluate the efficacy, safety, and tolerability of the drug NBI-1070770 in improving symptoms of major depressive disorder (MDD) compared to a placebo.
Neurocrine Biosciences is a biopharmaceutical company focused on developing treatments for neuropsychiatric, neurological, and neuroendocrine disorders, with a portfolio that includes FDA-approved therapies and a robust pipeline of clinical development programs.
Neurocrine Biosciences is currently conducting a study titled A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Maintenance of Effect of NBI-1065845 as an Adjunctive Treatment in Subjects With Major Depressive Disorder (MDD). The primary goal is to assess the efficacy of NBI-1065845 in delaying the relapse of depressive symptoms in individuals with MDD, highlighting its potential as a maintenance treatment.
Neurocrine Biosciences is launching a Phase 2 clinical study titled A Phase 2, Open-Label Study to Evaluate the Pharmacokinetics, Safety, Tolerability, and Pharmacodynamics of Crinecerfont in Pediatric Subjects 0 to <2 Years of Age With Congenital Adrenal Hyperplasia. The study aims to assess the pharmacokinetics of crinecerfont in young children with congenital adrenal hyperplasia (CAH), a significant step in addressing this rare condition.