Skip to content

A Phase 2, Multi-cohort Study Applying Innovative MRD Techniques for Transplant Eligible Participants with Previously Untreated Multiple Myeloma - TAURUS

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-505221-14-00
Acronym
EMN33
Enrollment
237
Registered
2023-11-07
Start date
2023-12-04
Completion date
Unknown
Last updated
2026-01-26

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

Conditions

Multiple Myeloma

Brief summary

The primary and secondary endpoints, and their respective timepoints are defined in Table 33 of the Protocol

Detailed description

The primary and secondary endpoints, and their respective timepoints are defined in Table 33 of the Protocol, Incidence and severity of AEs, adverse laboratory results, and other safety parameters following TEC-TAL, JNJ-79635322-D, and JNJ-79635322-DR administration.

Interventions

DRUGDEXAMETHASONE
DRUGVELCADE 3.5 mg powder for solution for injection
DRUGPARACETAMOL
DRUGteclistamab
DRUGDIPHENHYDRAMINE
DRUGDEXAMETHASONE SODIUM PHOSPHATE
DRUGDARZALEX 1800 mg solution for injection

Sponsors

European Myeloma Network B.V., Emn Trial Office S.r.l. Impresa Sociale
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The primary and secondary endpoints, and their respective timepoints are defined in Table 33 of the Protocol

Secondary

MeasureTime frame
The primary and secondary endpoints, and their respective timepoints are defined in Table 33 of the Protocol, Incidence and severity of AEs, adverse laboratory results, and other safety parameters following TEC-TAL, JNJ-79635322-D, and JNJ-79635322-DR administration.

Countries

Austria, Germany, Greece, Italy, Netherlands

Outcome results

None listed

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