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NCT07073547 · ClinicalTrials.gov registry record · Phase 1

A Phase I, Open-label, Multicenter Study to Evaluate the Safety, Tolerability, Cellular Kinetics, Immunogenicity, Pharmacodynamics, and Preliminary Efficacy of AZD0120 in Participants With Multiple Myeloma (DURGA-2)

A Phase 1 study of Multiple Myeloma, sponsored by AstraZeneca.

Recruiting
Registry status
Phase 1
Development phase
40
Enrollment target
13
Study locations

NCT07073547 is a Phase 1 study of Multiple Myeloma that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 40 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (93% lower). The trial reports 13 study locations across 12 states.

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The verdict

NCT07073547, a Phase 1 study of Multiple Myeloma, is actively recruiting participants, sponsored by AstraZeneca.

RECRUITING
Registry status
Phase 1
Development phase
40 participants
Enrollment target
13
Study locations

Study Summary

This is an interventional, modular, open-label, multicenter study to primarily evaluate the safety and tolerability of AZD0120 in adult participants with multiple myeloma (MM).

Conditions Studied

Interventions

  • BIOLOGICAL AZD0120

Study Locations (13)

Texas

  • Research Site - Dallas
  • Research Site - Houston

Arizona

  • Research Site - Phoenix

California

  • Research Site - Duarte

Colorado

  • Research Site - Denver

Florida

  • Research Site - Tampa

Georgia

  • Research Site - Atlanta

Iowa

  • Research Site - Iowa City

Minnesota

  • Research Site - Rochester

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2025-07-31
Est. Completion 2028-05-26
Phase Phase 1

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT07073547

The ClinicalTrials.gov registry entry for NCT07073547 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (93% lower). The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention - of which AZD0120 is the first listed.

NCT07073547 reports 13 study locations spanning 12 distinct geographic areas - top geographies include Texas, Arizona, California.

Frequently Asked Questions

What is clinical trial NCT07073547 about?

NCT07073547 is a clinical study titled "A Phase I, Open-label, Multicenter Study to Evaluate the Safety, Tolerability, Cellular Kinetics, Immunogenicity, Pharmacodynamics, and Preliminary Efficacy of AZD0120 in Participants With Multiple Myeloma (DURGA-2)". This is an interventional, modular, open-label, multicenter study to primarily evaluate the safety and tolerability of AZD0120 in adult participants with multiple myeloma (MM).

What is the current status of trial NCT07073547?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2025-07-31. Estimated completion is 2028-05-26.

What conditions does trial NCT07073547 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT07073547?

The interventions under investigation include: AZD0120 (BIOLOGICAL).

Who is sponsoring clinical trial NCT07073547?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07073547 being conducted?

This trial has 13 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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