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Dec 31, 2021

Leap Therapeutics Q4 2021 Earnings Report

Leap Therapeutics reported financial results for Q4 2021, featuring updates on DKN-01 development and strategic collaborations.

Key Takeaways

Leap Therapeutics reported Q4 2021 financial results, highlighting DKN-01 development and a strategic collaboration with BeiGene. License revenues were $0.4 million. Research and development expenses were $8.1 million, and general and administrative expenses were $2.8 million. Cash and cash equivalents totaled $114.9 million at the end of the year.

Leap Therapeutics presented positive data from the DisTinGuish clinical trial, demonstrating efficacy in G/GEJ cancer patients with high tumoral DKK1 expression.

The company is well-funded to advance DKN-01 into the next stages of development in G/GEJ and other cancers.

Leap Therapeutics will present updated data from the DisTinGuish Study in the second half of 2022.

DKN-01 modulates the Wnt/Beta-catenin and PI3kinase/AKT signaling pathways, playing a role in tumor cell signaling.

Total Revenue
$375K
Previous year: $375K
+0.0%
EPS
-$1
Previous year: -$0.9
+11.1%
Gross Profit
$375
Previous year: $375K
-99.9%
Cash and Equivalents
$115M
Previous year: $52.1M
+120.5%
Total Assets
$118M
Previous year: $54.4M
+116.9%

Leap Therapeutics

Leap Therapeutics

Forward Guidance

Leap Therapeutics is focused on developing targeted and immuno-oncology therapeutics and expects to advance DKN-01.

Positive Outlook

  • Advancing DKN-01 into next stages of development.
  • Presenting updated data from the DisTinGuish Study in the second half of 2022.
  • Strategic collaboration with BeiGene for DKN-01 development in Asia (excluding Japan), Australia, and New Zealand.
  • DKN-01 is in clinical trials in patients with esophagogastric, hepatobiliary, gynecologic, and prostate cancers.
  • Well funded to advance DKN-01

Challenges Ahead

  • Clinical trials may not have an effective design or generate positive results.
  • Potential delays or adverse effects due to COVID-19 related issues.
  • Unstable global market and economic conditions.
  • Uncertainties in the clinical development process.
  • Ability to obtain and maintain regulatory approval of drug product candidates.