CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 201 enrolled
Drug / intervention
Patient Reported Outcomesother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05831787
NCT05831787N/ACompleted

Monitoring SARS-CoV-2 Vaccines and COVID-19 Related Outcomes in Individuals With Multiple Myeloma

ASH Research Collaborative·observational·Posted Apr 26, 2023·Updated May 18, 2026

In Brief

An observational study evaluating Patient Reported Outcomes for Multiple Myeloma. Completed, enrolled 201 participants across 2 sites.

Detailed Summary

The COVID-19 pandemic has had an outsized impact on individuals with underlying social and medical vulnerability, leading to increased rates of severe disease, hospitalization, and death in these groups. Participants with underlying immune compromise, such as those with multiple myeloma, represent one such group. The advent of vaccines against SARS-CoV-2 has significantly limited morbidity and mortality across all groups, but the effectiveness of vaccination in individuals who are less likely to mount sufficient antibody response is uncertain. For this reason, booster vaccines have been recommended for those with underlying immune compromise. However, several key gaps remain in our understanding of how to best protect these individuals. There is a dearth of real-world evidence about the effectiveness of vaccination and boosters in patients who are immunocompromised, and very little information specifically about the recently approved mRNA boosters. Additionally, rates of vaccination and booster uptake in the United States remain low. A rapid, decentralized method of ascertaining information related to booster vaccine response and adverse events related to vaccines and COVID-19 infection is critical not only to answer questions about the booster vaccines, but to develop an infrastructure for answering similar questions about future vaccines or other diseases.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsModernaTX, Inc.

Timeline

N/ACompletedFinished
202420252026
First PostedApr 26, 2023
Enrollment StartJan 23, 2024
Primary CompletionDec 31, 2024
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 3.2 years ago

Interventions

Patient Reported Outcomesother

Patients will be asked to complete baseline, 30-day, and 6-month clinical and patient reported outcome health surveys.