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Mar 31, 2024

Tscan Therapeutics Q1 2024 Earnings Report

TScan Therapeutics reported financial results for the first quarter ended March 31, 2024, and provided a corporate update.

Key Takeaways

TScan Therapeutics reported a revenue of $0.6 million and a net loss of $30.1 million for the first quarter of 2024. The company dosed the first patient in its Phase 1 solid tumor program and closed an upsized public offering with gross proceeds of $167.8 million, extending the company's cash runway into the fourth quarter of 2026.

First patient dosed in Phase 1 clinical trial for the treatment of solid tumors; initial data anticipated in 2024.

All treatment-arm patients in the Phase 1 heme program remain relapse-free with no detectable disease, with a median follow-up of >10 months.

Closed upsized underwritten public offering with gross proceeds of $167.8 million, extending runway into the fourth quarter of 2026.

The Company expects to complete Phase 1 enrollment and open expansion cohorts at the proposed recommended Phase 2 dose in the third quarter of 2024 and provide a data update near the end of 2024.

Total Revenue
$566K
Previous year: $6.8M
-91.7%
EPS
-$0.32
Previous year: -$0.93
-65.6%
Gross Profit
-$688K
Previous year: $5.3M
-113.0%
Cash and Equivalents
$141M
Previous year: $95.6M
+47.0%
Free Cash Flow
-$30M
Previous year: -$24.4M
+22.7%
Total Assets
$241M
Previous year: $174M
+38.7%

Tscan Therapeutics

Tscan Therapeutics

Tscan Therapeutics Revenue by Segment

Forward Guidance

TScan anticipates several milestones for its Heme Malignancies Program and Solid Tumor Program.

Positive Outlook

  • Opening of expansion cohorts at the proposed recommended Phase 2 dose level to further characterize safety and evaluate translational and efficacy endpoints is planned for the third quarter of 2024.
  • Completion of Phase 1 enrollment and reporting of one-year clinical and translational data on initial patients is anticipated in the second half of 2024.
  • Expects to initiate registration trial pending feedback from regulatory authorities and report two-year clinical and translational data in 2025.
  • Phase 1 solid tumor clinical study has been initiated; first patient dosed in early May, with three additional patients enrolled and manufacturing underway.
  • Initial data expected in the second half of 2024.