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Cerevel Therapeutics Hldng Stock Price, News & Analysis

CERE NASDAQ

Company Description

Cerevel Therapeutics Holdings, Inc. (formerly Nasdaq: CERE) was a biopharmaceutical company dedicated to unraveling the mysteries of the brain to treat neuroscience diseases. The company focused on discovering and developing investigational therapies for a range of neurological and psychiatric conditions. According to multiple company communications, Cerevel combined deep expertise in neurocircuitry with a focus on targeted receptor subtype selectivity and a differentiated approach to pharmacology to build its pipeline. Cerevel was headquartered in Cambridge, Massachusetts.

Cerevel developed a diversified pipeline of clinical-stage and preclinical product candidates with potential applications in schizophrenia, Alzheimer’s disease psychosis, epilepsy, panic disorder, and Parkinson’s disease. Its programs included several receptor-targeted small molecules designed to modulate specific pathways in the central nervous system. The company described five clinical-stage investigational therapies and several preclinical compounds in development across these neuroscience indications.

Acquisition by AbbVie

On December 6, 2023, AbbVie Inc. and Cerevel Therapeutics announced a definitive agreement under which AbbVie would acquire Cerevel. Under the terms of the transaction, AbbVie agreed to acquire all outstanding shares of Cerevel for $45.00 per share in cash, valuing Cerevel at a total equity value of approximately $8.7 billion. The boards of directors of both companies approved the transaction, which was expected to close in the middle of 2024, subject to shareholder and regulatory approvals and other customary closing conditions.

On August 1, 2024, AbbVie announced that it had completed its acquisition of Cerevel Therapeutics. With the completion of the acquisition, Cerevel became part of AbbVie, and AbbVie stated that Cerevel’s common stock was expected to cease trading on the Nasdaq stock exchange prior to market open on August 1, 2024. AbbVie described Cerevel as a strong strategic fit that complements AbbVie’s existing neuroscience portfolio in psychiatry, migraine, Parkinson’s disease and other neurological and psychiatric disorders.

Neuroscience Pipeline and Key Programs

Cerevel’s pipeline, as described in its public communications prior to the acquisition, included multiple clinical-stage assets targeting specific receptor systems in the brain:

  • Emraclidine: An M4-selective positive allosteric modulator (PAM) in development for schizophrenia and Alzheimer’s disease psychosis. Cerevel conducted two placebo-controlled Phase 2 trials in schizophrenia (EMPOWER-1 and EMPOWER-2) and a 52-week open-label safety extension (EMPOWER-3). The company also initiated a Phase 1 multiple ascending dose trial in elderly healthy volunteers to support development in Alzheimer’s disease psychosis, and reported that the U.S. Food and Drug Administration had granted Fast Track designation for emraclidine for hallucinations and delusions associated with Alzheimer’s disease psychosis.
  • Tavapadon: A D1/D5 partial agonist in Phase 3 development for the treatment of Parkinson’s disease. Cerevel described tavapadon as having the potential to be a first-in-class D1/D5 selective partial agonist for Parkinson’s disease, studied both as monotherapy and as adjunctive treatment to levodopa. The Phase 3 TEMPO clinical development program included two monotherapy trials (TEMPO-1 and TEMPO-2), one adjunctive trial (TEMPO-3), and an open-label extension (TEMPO-4).
  • Darigabat: An α2/3/5-selective GABAA receptor PAM under development for epilepsy and panic disorder. Cerevel conducted the REALIZE Phase 2 proof-of-concept trial in focal epilepsy, with a corresponding open-label safety extension, and initiated the ADAPT Phase 2 proof-of-concept trial in panic disorder.
  • CVL-871: A D1/D5 partial agonist in a Phase 2a exploratory trial for treatment of dementia-related apathy.
  • CVL-354: A selective kappa opioid receptor antagonist (KORA) in development for major depressive disorder and substance use disorder.

In addition to these lead programs, Cerevel reported early clinical and discovery-stage efforts, including a selective M4 agonist program for psychiatric and neurological indications and a selective PDE4 inhibitor (PDE4D-sparing) program for psychiatric, neuroinflammatory and other disorders.

Therapeutic Focus Areas

Cerevel’s work targeted several major neuroscience diseases:

  • Schizophrenia and other psychiatric conditions, through emraclidine and other receptor-targeted candidates.
  • Parkinson’s disease, through tavapadon and related D1/D5 receptor agonist approaches, including both monotherapy and adjunctive treatment strategies.
  • Epilepsy and panic disorder, through darigabat and its modulation of specific GABAA receptor subtypes.
  • Alzheimer’s disease psychosis and dementia-related apathy, through emraclidine and CVL-871.
  • Mood disorders and major depressive disorder, through CVL-354 and other early-stage programs.

AbbVie highlighted that Cerevel’s clinical-stage assets, including emraclidine, tavapadon, CVL-354 and darigabat, are complementary to AbbVie’s existing neuroscience portfolio and may address areas of significant unmet need in psychiatric and neurological disorders.

Business Model and Operations

Based on its public disclosures, Cerevel operated as a clinical-stage biopharmaceutical company. It generated value by advancing a portfolio of investigational neuroscience therapies through clinical development, with the goal of obtaining regulatory approvals in multiple indications. The company emphasized its deep understanding of neurocircuitry and receptor subtype selectivity as a foundation for its research and development programs. Cerevel also referenced internal research efforts, external collaborations and potential acquisitions as avenues to explore new modalities and expand its pipeline.

As a publicly traded company prior to its acquisition, Cerevel raised capital through equity offerings. For example, in October 2023 the company announced the pricing of a public offering of common stock, stating that the net proceeds were expected to support planned data readouts and fund operations into 2026.

Status as a Former Public Company

Following the completion of AbbVie’s acquisition on August 1, 2024, Cerevel Therapeutics became part of AbbVie and its common stock was expected to cease trading on Nasdaq. As a result, the CERE ticker represents a former standalone public company whose neuroscience assets and operations have been integrated into AbbVie’s broader neuroscience franchise. Historical information about Cerevel’s programs, trials and corporate activities remains relevant for understanding the origin and development of these assets within AbbVie’s pipeline.

FAQs about Cerevel Therapeutics (CERE)

Stock Performance

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Last updated:
-100%
Performance 1 year

SEC Filings

No SEC filings available for Cerevel Therapeutics Hldng.

Financial Highlights

$0
Revenue (TTM)
-$131,912,000
Net Income (TTM)
-$119,669,000
Operating Cash Flow
-$142,656,000

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Frequently Asked Questions

What is the current stock price of Cerevel Therapeutics Hldng (CERE)?

The current stock price of Cerevel Therapeutics Hldng (CERE) is $43.44 as of February 7, 2025.

What is the market cap of Cerevel Therapeutics Hldng (CERE)?

The market cap of Cerevel Therapeutics Hldng (CERE) is approximately 8.2B. Learn more about what market capitalization means .

What is the revenue (TTM) of Cerevel Therapeutics Hldng (CERE) stock?

The trailing twelve months (TTM) revenue of Cerevel Therapeutics Hldng (CERE) is $0.

What is the net income of Cerevel Therapeutics Hldng (CERE)?

The trailing twelve months (TTM) net income of Cerevel Therapeutics Hldng (CERE) is -$131,912,000.

What is the earnings per share (EPS) of Cerevel Therapeutics Hldng (CERE)?

The diluted earnings per share (EPS) of Cerevel Therapeutics Hldng (CERE) is -$0.73 on a trailing twelve months (TTM) basis. Learn more about EPS .

What is the operating cash flow of Cerevel Therapeutics Hldng (CERE)?

The operating cash flow of Cerevel Therapeutics Hldng (CERE) is -$119,669,000. Learn about cash flow.

What is the current ratio of Cerevel Therapeutics Hldng (CERE)?

The current ratio of Cerevel Therapeutics Hldng (CERE) is 10.22, indicating the company's ability to pay short-term obligations. Learn about liquidity ratios.

What is the operating income of Cerevel Therapeutics Hldng (CERE)?

The operating income of Cerevel Therapeutics Hldng (CERE) is -$142,656,000. Learn about operating income.

What was Cerevel Therapeutics’ core business focus?

Cerevel Therapeutics focused on discovering and developing investigational therapies for neuroscience diseases. The company described itself as dedicated to unraveling the mysteries of the brain, combining deep expertise in neurocircuitry with targeted receptor subtype selectivity and a differentiated approach to pharmacology.

Which diseases did Cerevel Therapeutics target with its pipeline?

Cerevel reported a diversified pipeline aimed at treating schizophrenia, Alzheimer’s disease psychosis, epilepsy, panic disorder, Parkinson’s disease, mood disorders, major depressive disorder, substance use disorder and dementia-related apathy, through multiple clinical-stage and preclinical programs.

What were Cerevel’s key clinical-stage drug candidates?

Public disclosures identified several lead programs: emraclidine, an M4-selective positive allosteric modulator for schizophrenia and Alzheimer’s disease psychosis; tavapadon, a D1/D5 partial agonist in Phase 3 for Parkinson’s disease; darigabat, an α2/3/5-selective GABAA receptor PAM for epilepsy and panic disorder; CVL-871, a D1/D5 partial agonist for dementia-related apathy; and CVL-354, a selective kappa opioid receptor antagonist for major depressive disorder and substance use disorder.

Where was Cerevel Therapeutics headquartered?

Cerevel Therapeutics stated that it was headquartered in Cambridge, Massachusetts. This location was cited in multiple company press releases describing its corporate profile.

What happened to Cerevel Therapeutics’ stock ticker CERE?

AbbVie announced on August 1, 2024 that it had completed its acquisition of Cerevel Therapeutics. AbbVie stated that Cerevel’s common stock was expected to cease trading on the Nasdaq stock exchange prior to market open on that date. After the closing of the transaction, CERE represents a former standalone public company that has been integrated into AbbVie.

How did AbbVie describe the strategic rationale for acquiring Cerevel?

AbbVie stated that Cerevel’s clinical-stage assets complement AbbVie’s emerging neuroscience pipeline and on-market brands in psychiatry, migraine and Parkinson’s disease. AbbVie characterized Cerevel as a strong strategic fit that strengthens its foundation in neuroscience and adds a robust pipeline of assets focused on psychiatric and neurological disorders where significant unmet needs remain.

What is emraclidine and what indications was it being studied for?

Emraclidine is described as an M4-selective positive allosteric modulator. Cerevel reported that it was conducting two placebo-controlled Phase 2 trials in schizophrenia (EMPOWER-1 and EMPOWER-2), along with a 52-week open-label safety extension (EMPOWER-3). The company also initiated a Phase 1 multiple ascending dose trial in elderly healthy volunteers to support development in Alzheimer’s disease psychosis, and noted that the FDA granted Fast Track designation for emraclidine for hallucinations and delusions associated with Alzheimer’s disease psychosis.

What is tavapadon and how was it being evaluated in Parkinson’s disease?

Tavapadon is a D1/D5 partial agonist in development for Parkinson’s disease. Cerevel described it as having the potential to be a first-in-class D1/D5 selective partial agonist, studied as both monotherapy and adjunctive treatment to levodopa. The Phase 3 TEMPO program included two monotherapy trials (TEMPO-1 and TEMPO-2), one adjunctive trial (TEMPO-3) and an open-label extension (TEMPO-4). Cerevel later announced positive topline results from the pivotal Phase 3 TEMPO-3 adjunctive trial in people living with Parkinson’s disease.

How did Cerevel support its research and development activities financially?

As a public company, Cerevel raised capital through equity offerings. For example, in October 2023 it announced the pricing of an underwritten public offering of common stock, stating that the net proceeds were expected to support planned data readouts in 2024 and fund operations into 2026. The company also reported its cash, cash equivalents and marketable securities position in quarterly financial results.

Does Cerevel Therapeutics still operate as an independent company?

Based on AbbVie’s announcement on August 1, 2024, Cerevel Therapeutics became part of AbbVie upon completion of the acquisition. AbbVie indicated that Cerevel’s common stock would cease trading on Nasdaq in connection with the closing. Cerevel’s programs and employees were described as joining AbbVie’s neuroscience organization rather than continuing as a separate public entity.