Cypherpunk Technologies Records $77.2M Q1 Net Loss on ZEC Decline.
ZcashTracker
Key Takeaways
- Cypherpunk Technologies increased its Zcash treasury to 314,185.70 ZEC by May 13, 2026, representing approximately 1.88% of the total circulating supply.
- The company acquired an additional 10,279.30 ZEC for $5 million between April 15 and May 13, 2026, at an average purchase price of $486.41 per ZEC.
- Cypherpunk invested $5 million in Zcash Open Development Labs (ZODL), the core developers of the Zcash Network and Zodl wallet, in March 2026.
- A net loss of $77.2 million was reported for the first quarter of 2026, primarily due to a $77.6 million unrealized loss on ZEC treasury holdings.
- As of March 31, 2026, ZEC treasury holdings were valued at $73.8 million, based on a ZEC price of $240.47.
- Cypherpunk's Leap Therapeutics subsidiary received FDA Fast Track designation for sirexatamab and presented positive DKK1 biomarker assay and DeFianCe study results for metastatic colorectal cancer at AACR 2026.
Leap Therapeutics Subsidiary Developments
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Cypherpunk's biotechnology subsidiary, Leap Therapeutics, made significant progress in its oncology pipeline. In May 2026, the U.S. Food and Drug Administration (FDA) granted Fast Track designation to sirexatamab. This designation applies to sirexatamab in combination with specific chemotherapy regimens and bevacizumab, for treating DKK1-high metastatic colorectal cancer patients whose disease has progressed after one prior systemic therapy. The Fast Track program facilitates development and expedites review for drugs addressing serious conditions with unmet medical needs.
At the American Association for Cancer Research (AACR) 2026 in April, Leap Therapeutics presented a new plasma DKK1 biomarker assay. This assay is designed as a companion diagnostic to identify patients likely to benefit from sirexatamab, an anti-DKK1 monoclonal antibody. Results from Part B of the DeFianCe study, a Phase 2 trial of sirexatamab in combination with bevacizumab and chemotherapy for microsatellite stable colorectal cancer patients, were also presented.
In the DeFianCe study, sirexatamab demonstrated statistically significant benefits in overall response rate (ORR) and overall survival (OS) for patients with high DKK1 levels (>380 pg/ml). Among this subgroup (n=87), ORR was 42% in the sirexatamab arm (including one complete response) versus 16% in the control arm (p=0.003). Median OS (mOS) was not reached in the sirexatamab arm compared to 14.39 months in the control arm (HR 0.47, p=0.0244).
