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Solid Biosciences Inc. SLDB SGT501 — Research And Development Expense
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Where this comes from
Reported directly by Solid Biosciences Inc. in its filing.
Tagged under the XBRL concept us-gaap:ResearchAndDevelopmentExpense.
The source filing: Solid Biosciences Inc.’s 10-Q, filed August 6, 2026.
- Filed
- Aug 6, 2026, 4:04 PM EDT
- Fiscal quarter
- Q2 FY2026
- Calendar quarter
- Q2 2026
- Accession
- 0001193125-26-337935
| Line item | Three Months Ended June 30, 2026 | Three Months Ended June 30, 2025 | Six Months Ended June 30, 2026 | Six Months Ended June 30, 2025 |
|---|---|---|---|---|
| Segment expenses: | ||||
| SGT-003 | $24,516 | $12,219 | $47,458 | $21,385 |
| SGT-501 | 903 | 2,223 | 2,310 | 6,689 |
| SGT-212 | 2,364 | 1,145 | 5,680 | 1,970 |
| External R&D other | 1,983 | 3,116 | 4,840 | 5,886 |
| Internal R&D expense(1) | 9,060 | 6,765 | 18,211 | 13,608 |
| External G&A expense | 6,327 | 5,279 | 11,795 | 10,156 |
| Internal G&A expense(1) | 4,734 | 3,360 | 8,600 | 6,823 |
Item 1. Financial Statements (unaudited)
FAQ
- What is Solid Biosciences Inc.'s SGT501 — research and development expense?
- Solid Biosciences Inc. (SLDB) reported SGT501 — research and development expense of $903K in Q2 2026.
- How has Solid Biosciences Inc.'s SGT501 — research and development expense changed year-over-year?
- Solid Biosciences Inc.'s SGT501 — research and development expense decreased by 59.4% year-over-year, from $2.22M to $903K.
- What is the long-term trend for Solid Biosciences Inc.'s SGT501 — research and development expense?
- Over 2 years (2023 to 2025), Solid Biosciences Inc.'s SGT501 — research and development expense has grown at a 73.6% compound annual growth rate (CAGR), from $3.2M to $9.64M.
- What does SGT501 — research and development expense mean?
- This metric represents the total costs incurred specifically for the research, clinical development, and manufacturing process optimization of the SGT501 gene therapy candidate. It captures the investment required to advance this specific therapeutic program through preclinical studies and clinical trials toward potential regulatory approval. Tracking this expense provides insight into the company's capital allocation strategy and the progress of its core pipeline assets.
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