| 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 |
|---|---|---|---|---|---|---|---|
| ― | $14.28B | 34.20 | 14.96% | ― | 19.61% | 11.36% | |
| ― | $11.25B | 16.27 | 17.72% | 0.69% | 10.63% | 6.35% | |
| ― | $1.19B | 9.55 | 18.32% | ― | 1.37% | -18.10% | |
| ― | $23.22B | ― | -2.31% | ― | 2.43% | 64.37% | |
| ― | $11.96B | ― | -19.77% | 4.63% | -7.47% | -438.39% | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
| ― | $960.66M | ― | -15.57% | ― | 2.25% | -301.59% |
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.
Neurocrine Biosciences is conducting a Phase 3 clinical study titled ‘NBI-1117568-SCZ3029: Evaluation of NBI-1117568 in Inpatient Adults With Schizophrenia.’ The study aims to assess the efficacy, safety, and tolerability of NBI-1117568, a drug intended to improve behavioral and psychological symptoms in adults with schizophrenia who require inpatient care.
Neurocrine Biosciences is conducting a Phase 3 clinical study titled ‘A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Dyskinesia Due to Cerebral Palsy.’ The study aims to evaluate the effectiveness of valbenazine in reducing chorea in individuals with dyskinesia caused by cerebral palsy, a significant step in addressing movement disorders in this population.
Neurocrine Biosciences is conducting a long-term study titled ‘A Long-Term, Open-Label Study to Assess the Safety and Tolerability of NBI-1065845 as Adjunctive Treatment in Subjects With Major Depressive Disorder (MDD).’ The study aims to evaluate the safety and tolerability of NBI-1065845 when used alongside standard treatments for MDD, a significant mental health condition affecting millions globally.
Neurocrine Biosciences’ recent earnings call showcased a robust commercial performance, marked by significant revenue growth and successful product launches. The company is making strides in expanding its market presence and advancing its pipeline, although it faces challenges from pricing pressures and regulatory uncertainties.