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A Phase 1 Open-label, Multicenter, Dose Escalation Study of the Safety, Tolerability, and Pharmacokinetics of HPN217 in Patients with Relapsed/Refractory Multiple Myeloma

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515582-33-00
Acronym
MK-4002-001
Enrollment
10
Registered
2024-09-11
Start date
2020-10-26
Completion date
Unknown
Last updated
2025-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Multiple Myeloma that does not respond to treatment, Relapsed/Refractory Multiple Myeloma (RRMM)

Interventions

None listed

Sponsors

Harpoon Therapeutics Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

France, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026