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MapLight Therapeutics, Inc. MPLT Clinical Trial — Research And Development Expense
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Where this comes from
Reported directly by MapLight Therapeutics, Inc. in its filing.
Tagged under the XBRL concept us-gaap:ResearchAndDevelopmentExpense.
The source filing: MapLight Therapeutics, Inc.’s 10-Q, filed May 14, 2026.
- Filed
- May 14, 2026, 4:25 PM EDT
- Fiscal quarter
- Q1 FY2026
- Calendar quarter
- Q1 2026
- Accession
- 0001193125-26-224129
| Line item | Three Months Ended March 31, 2026 | Three Months Ended March 31, 2025 |
|---|---|---|
| Clinical trial expenses | $24,819 | $1,939 |
| Employee-related research and development expenses | 15,993 | 7,050 |
| Chemistry, manufacturing and controls expenses | 6,417 | 3,956 |
| Preclinical program expenses | 5,522 | 6,081 |
| Other research and development expenses | 933 | 761 |
| Employee-related general and administrative expenses | 6,990 | 2,060 |
| Professional fees and other general and administrative expenses | 3,829 | 1,696 |
| Other segment items(1) | (3,835) | (1,203) |
Item 1. Financial Statements.
FAQ
- What is MapLight Therapeutics, Inc.'s clinical trial — research and development expense?
- MapLight Therapeutics, Inc. (MPLT) reported clinical trial — research and development expense of $24.82M in Q1 2026.
- How has MapLight Therapeutics, Inc.'s clinical trial — research and development expense changed year-over-year?
- MapLight Therapeutics, Inc.'s clinical trial — research and development expense increased by 1180.0% year-over-year, from $1.94M to $24.82M.
- What does clinical trial — research and development expense mean?
- This metric represents the total costs incurred by the company specifically attributed to the research and development activities within its clinical trial segment. It captures expenditures related to drug discovery, preclinical studies, and the execution of clinical trials for therapeutic candidates. Monitoring this expense provides insight into the company's investment intensity in its pipeline development and its commitment to advancing clinical-stage assets toward regulatory approval.
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