CytoDyn
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CytoDyn (CYDY) investor relations material

CytoDyn Study update summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Study update summary30 Apr, 2026

Study background and design

  • CLOVER Phase II study in metastatic colorectal cancer enrolled 60 patients, all with advanced, heavily pretreated disease.

  • Patients received leronlimab plus Lonsurf and Avastin, randomized to 350 mg or 700 mg doses.

  • 100% of screened patients were CCR5 positive, expediting enrollment and broadening eligibility.

  • No grade 3/4 adverse events or dose-limiting toxicities attributed to leronlimab.

  • Two data safety monitoring board reviews found no safety concerns.

Key efficacy and biomarker findings

  • All 19 initial patients showed ctDNA declines, with a median 70% decrease at week 2.

  • 68% of 22 patients with RECIST data at week 8 had tumor shrinkage or stable disease.

  • ctDNA reductions were observed even in patients with KRAS mutations, typically hard to treat.

  • Four patients achieved undetectable ctDNA during follow-up, three on the lower dose.

  • Numeric increases in PD-L1 were observed in most patients, suggesting immune activation.

Clinical and patient-reported outcomes

  • Early clinical improvements included reduced pain and improved performance status.

  • Some patients returned to work due to improved well-being.

  • Repeat biopsies showed decreased tumor cellularity and increased PD-L1 expression.

  • Liquid biopsy (ctDNA) provided rapid, sensitive response readouts, often preceding scan changes.

  • The backbone regimen alone historically yields low response rates (<6%).

Significance of ctDNA declines in CLOVER study
Breakthrough designation application timeline
Leronlimab efficacy in KRAS mutant CRC patients
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