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MapLight Therapeutics MPLT · USD

Health Care · US listing · 🇺🇸 United States

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7.28

+5.05%

Close of 9 Nov 2026, in USD

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About MapLight Therapeutics

From its filings with the US Securities and Exchange Commission

SEC filings

MapLight Therapeutics is based in Redwood City, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker MPLT. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported a net loss of $161.2m. At that date it held total assets of $479.5m and shareholders' equity of $458.4m.

In its own words

We are a clinical-stage biopharmaceutical company focused on improving the lives of patients suffering from debilitating central nervous system, or CNS, disorders. We were founded by globally recognized leaders in psychiatry and neuroscience research to address the lack of circuit-specific pharmacotherapies available for patients. Our discovery platform holds the potential to fill this void by identifying neural circuits causally linked to disease and targeting those circuits for therapeutic modulation. We believe our deep understanding of these causal links between the modulation of defined neural circuits and the resulting changes in disease-specific behaviors will enable us to develop therapeutics that can deliver efficacy, safety, tolerability and ease-of-use advantages to patients and prescribers.

Our lead product candidate, ML-007C-MA, is a fixed-dose combination of an M1/M4 muscarinic agonist, ML-007, co-formulated with a peripherally acting anticholinergic, or PAC, which we are initially developing for the treatment of schizophrenia and Alzheimer's disease psychosis, or ADP. ML-007C-MA is designed to activate both M1 and M4 muscarinic receptors centrally to drive efficacy, while synchronizing the pharmacokinetics of the agonist and antagonist components to mitigate peripheral cholinergic side effects. ML-007 alone, co-administered, or co-formulated with PAC has been evaluated in four Phase 1 trials, with a total of 270 healthy participants enrolled and more than 1,500 doses of ML-007 administered.

Quoted from its 10-K, filed 26 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
27 Oct 2025
Employees
133
Head office
800 CHESAPEAKE DRIVE, REDWOOD CITY, CA, 94063
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Non-accelerated filer<br>Smaller reporting company<br>Emerging growth company

Leadership

Pay as last reported

  • Dr. Christopher KroegerCo-Founder, President, Chief Executive Officer, Director, since 2018$8.8m
  • Mr. Vishwas SetiaChief Financial Officer$3.1m
  • Mr. Jonathan GillisChief Accounting Officer, Chief Administrative Officer
  • Mr. James LillieChief Scientific Officer
  • Mr. Kristopher HansonGeneral Counsel
  • Ms. Erin FoffChief Medical Officer$2.8m
  • Dr. Anatol KreitzerChief Discovery Officer
  • Mr. Robert MalenkaDirector, since 2018$3.1m
  • Dr. Timothy GarnettIndependent Director$277,055
  • Ms. Nanna LuneborgIndependent Director
  • Mr. George PavlovIndependent Director
  • Mr. Jim TrenkleIndependent Director

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
0
Environment
0
Social
0
Governance
0

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Headquartered in Redwood City, California, a biotech hub.
  • Focus on developing therapeutics for brain disorders with a lead product ML-007C-MA.
  • Company has a clinical-stage pipeline including two product candidates and two preclinical programs.

Weaknesses

  • IPO scheduled for 2025-10-27, indicating limited current market presence.
  • No information provided on current revenue or financial performance.
  • Dependent on the success of clinical-stage products with no commercialized drugs yet.

Opportunities

  • Potential market for ML-007C-MA in schizophrenia and Alzheimer’s disease psychosis.
  • ML-004 could address social communication deficits in autism spectrum disorder.
  • Expansion of preclinical programs ML-021 and ML-009 into clinical development.

Threats

  • Risk of failure in clinical trials for ML-007C-MA and ML-004.
  • Competition from other biotech firms in CNS disorder treatments.
  • Regulatory hurdles for approval of novel therapeutics in CNS disorders.

Sources and methodology

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