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Jun 30, 2023

Tscan Therapeutics Q2 2023 Earnings Report

TScan Therapeutics reported financial results for the second quarter ended June 30, 2023, and provided a corporate update.

Key Takeaways

TScan Therapeutics reported a net loss of $24.0 million for the second quarter ended June 30, 2023, compared to a net loss of $15.1 million for the same period in 2022. The company ended the quarter with $208.8 million in cash and cash equivalents. Revenue for the quarter was $3.1 million, compared to $4.1 million for the second quarter ended June 30, 2022.

Presented preliminary Phase 1 clinical data from heme malignancies trial at the ASGCT 26th Annual Meeting.

Announced FDA clearance of fourth IND for solid tumor program – TSC-200-A0201 targeting HPV16.

Closed underwritten public offering with net proceeds of approximately $134.7 million.

Ended 2Q 2023 with cash and cash equivalents of $208.8 million, which along with $30 million proceeds from Amgen, will fund the Company into 2026.

Total Revenue
$3.15M
Previous year: $4.06M
-22.4%
EPS
-$0.51
Previous year: -$0.63
-19.0%
Gross Profit
$1.85M
Previous year: $2.85M
-35.0%
Cash and Equivalents
$209M
Previous year: $126M
+66.3%
Free Cash Flow
-$22.4M
Previous year: -$15.3M
+47.1%
Total Assets
$317M
Previous year: $152M
+107.9%

Tscan Therapeutics

Tscan Therapeutics

Tscan Therapeutics Revenue by Segment

Forward Guidance

TScan Therapeutics anticipates reaching the recommended Phase 2 dose for both TSC-100 and TSC-101 and reporting interim clinical data for the program by the end of 2023. The company also plans to initiate a Phase 1 solid tumor clinical study in the second half of 2023 and anticipates sharing preliminary data by the end of 2023.

Positive Outlook

  • Expects to reach the recommended Phase 2 dose for both TSC-100 and TSC-101 and report interim clinical data for the program by the end of 2023.
  • Plans to complete Phase 1 dosing and report prevention of relapse data in 2024.
  • Anticipates further expansion of the ImmunoBank with the recent filing of an IND for TSC-203-A0201, an HLA-A*02:01-restricted TCR targeting PRAME, and IND filings for two additional TCRs by year-end.
  • Plans to initiate Phase 1 solid tumor clinical study in the second half of 2023 and anticipates sharing preliminary data by the end of 2023.
  • Expects to report initial multiplexed therapy data for its first combinations of TCR-Ts under T-Plex, as well as response data for singleplex cohorts, in 2024.