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A Phase 1/2a, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of HDP-101 in Patients With Plasma Cell Disorders Including Multiple Myeloma

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Trial Profile

A Phase 1/2a, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of HDP-101 in Patients With Plasma Cell Disorders Including Multiple Myeloma

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 16 Jul 2024

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At a glance

  • Drugs HDP 101 (Primary)
  • Indications Multiple myeloma
  • Focus Adverse reactions; First in man; Therapeutic Use
  • Sponsors Heidelberg Pharma AG
  • Most Recent Events

    • 11 Jul 2024 According to a Heidelberg Pharma AG media release, Cohort 6 will consist of three arms, with at least three patients enrolled in each arm. In consultation with the clinical investigators, the dose will be 90 µg/kg in order to test these three dosing regimens with as little risk to the patients as possible. Further cohorts are planned with the most promising dosing regimens from cohort 6 and an increase in dose levels.
    • 23 May 2024 According to a Heidelberg Pharma AG media release, company will be participating and presenting at 10th Annual Oncology Innovation Forum, ASCO Annual Meeting, BIO International Convention and Jefferies Global Healthcare Conference.
    • 12 May 2024 Planned number of patients changed from 78 to 130.
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