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Sep 30, 2021

Curis Q3 2021 Earnings Report

Curis reported financial results for the third quarter ended September 30, 2021 and provided business updates.

Key Takeaways

Curis reported a net loss of $11.1 million, or $0.12 per share, for the third quarter of 2021, compared to a net loss of $6.0 million, or $0.11 per share, for the same period in 2020. Revenues for the third quarter of 2021 were $3.0 million, compared to $2.7 million for the same period in 2020. The company's cash, cash equivalents and investments totaled $149.8 million as of September 30, 2021.

Advanced clinical trials of CA-4948, a small molecule IRAK4 inhibitor, across nine distinct patient populations.

Initiated dosing in the combination stage of the Phase 1/2 study of CA-4948 plus azacitidine and CA-4948 plus venetoclax.

New preclinical data highlighting the potential of CA-4948 in additional hematologic malignancies was presented.

Enrollment remains on track in the ongoing Phase 1 dose escalation study of CI-8993.

Total Revenue
$3.04M
Previous year: $2.74M
+10.8%
EPS
-$2.4
Previous year: -$2.2
+9.1%
Gross Profit
$2.89M
Previous year: $2.61M
+10.8%
Cash and Equivalents
$150M
Previous year: $23.6M
+536.1%
Free Cash Flow
-$9.61M
Previous year: -$6.04M
+59.2%
Total Assets
$172M
Previous year: $45.7M
+276.4%

Curis

Curis

Curis Revenue by Segment

Forward Guidance

Curis plans to provide a clinical data update in January from ongoing clinical studies, including safety data from the Phase 1 study of CI-8993 and the latest safety and efficacy data from the CA-4948 study in AML/MDS patients with spliceosome or FLT3 mutations.

Positive Outlook

  • Provide a clinical data update on ongoing studies in January.
  • Report initial safety data from the Phase 1 monotherapy study of CI-8993.
  • Share the latest safety and efficacy data from the Phase 1/2 monotherapy study of CA-4948 in AML/MDS patients.
  • Provide additional data from the ongoing Phase 1/2 monotherapy study of CA-4948 in patients with R/R AML/MDS at a medical meeting in the first half of the year.
  • Report initial data at a medical meeting from the ongoing Phase 1/2 combination study of CA-4948 plus ibrutinib in patients with B cell cancers in the first half of the year.