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FDA Clearance Moves Percheron's HMBD-002 AML Trial Toward Patients

8:17am on Monday 2nd of November, 2026 AEDT • Biotechnology
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FDA Clearance Moves Percheron's HMBD-002 AML Trial Toward Patients

8:17am on Monday 2nd of November, 2026 AEDT
Key Points
  • FDA clearance enables the Vanderbilt Health-led US trial to proceed
  • HMBD-002 to be tested with venetoclax and azacitidine
  • Study proposed to enrol up to 20 patients with relapsed or refractory disease
  • Clinical trial material has been manufactured and released
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