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Multiparametric Imaging in Multiple Myeloma

Multiparametric Imaging in Multiple Myeloma

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02646085
Enrollment
10
Registered
2016-01-05
Start date
2016-07-31
Completion date
2021-06-30
Last updated
2021-09-16

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

Conditions

Multiple Myeloma

Brief summary

Patients with Multiple Myeloma will undergo single timepoint Positron Emission Tomography imaging with intravenously injected C11 Methionine to detect viable lesions.

Interventions

DRUGC11 Methionine positron emission tomography

diagnostic positron emission tomography imaging after intravenous injection of C11 Methionine

Sponsors

Yingbing Wang
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Multiple Myeloma with symptomatic bone or soft tissue disease * Eastern Cooperative Oncology Group status 0 to 2 * Life expectance \>= 12 weeks * Ability to understand and willingness to sign informed consent * Tissue sampling with genotype data planned within 3 months of C11 positron emission tomography (PET) imaging

Exclusion criteria

* Pregnant or breast feeding * Claustrophobic reactions and unable to lie still on a bed inside the PET scanner for 60 minutes * Research related radiation exposure exceeding 50 millisieverts

Design outcomes

Primary

MeasureTime frameDescription
Quantitative measure of C11 Methionine uptake12 monthsStandardized uptake value (a semiquantitative, unit less measure of radioactivity normalized for injected activity and body weight) will be measured for individual C11 Methionine uptake abnormalities (defined as focally increased uptake higher than background levels in a similar tissue type). All abnormal uptake not in locations common for benign etiologies, such as fracture and degenerative change, will be measured.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026