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Jun 30, 2021

Tourmaline Bio Q2 2021 Earnings Report

Reported financial results for the second quarter of 2021 and provided a business update.

Key Takeaways

Talaris Therapeutics reported its Q2 2021 financial results, highlighting progress with FREEDOM-1 trial and plans for FREEDOM-2 and FREEDOM-3 trials. The company's cash, cash equivalents, and marketable securities totaled $266.2 million, expected to fund operations into 2025.

On track to provide FREEDOM-1 initial clinical update before year-end.

Plans to initiate FREEDOM-2 and FREEDOM-3 trials.

Expects to disclose additional indication for FCR001 before the end of the year.

Finished the second quarter with $266.2 million in cash, cash equivalents and marketable securities.

Total Revenue
$0
EPS
-$4.1
R&D Expenses
$7.6M
G&A Expenses
$3.5M
Cash and Equivalents
$266M
Free Cash Flow
-$11.3M
Total Assets
$273M

Tourmaline Bio

Tourmaline Bio

Forward Guidance

Talaris Therapeutics is focused on advancing its clinical trials, including FREEDOM-1, FREEDOM-2, and FREEDOM-3, and expects to announce an additional indication for FCR001 before the end of 2021.

Positive Outlook

  • On track to provide FREEDOM-1 initial clinical update later this year.
  • Expanding clinical trial footprint to 14 active sites in the United States.
  • Remains on track to initiate a Phase 2 (FREEDOM-2) trial for FCR001 in delayed tolerance induction in the fourth quarter of 2021.
  • Remains on track to initiate its first clinical trial in autoimmune diseases with its FREEDOM-3 trial in the fourth quarter of 2021.
  • Remains on track to announce an additional target indication for FCR001 relating to a severe non-malignant blood, immune or metabolic disorder before the end of 2021.

Challenges Ahead

  • Risks associated with the impact of COVID-19 on the timing and anticipated timing and results of its clinical trials.
  • Risk that the results of Talaris’ clinical trials may not be predictive of future results in connection with future clinical trials.
  • The Company’s ability to successfully demonstrate the safety and efficacy of its drug candidates.
  • The timing and outcome of Talaris’ planned interactions with regulatory authorities.
  • Obtaining, maintaining and protecting its intellectual property.