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Trial - NCT05028374


Column Value
Trial registration number NCT05028374
Full text link
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

First author
Last imported at : Aug. 30, 2022, 9:30 p.m.
Source : ClinicalTrials.gov

Not reported

Contact
Last imported at : Aug. 30, 2022, 9:30 p.m.
Source : ClinicalTrials.gov

Not reported

Registration date
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

2021-08-31

Recruitment status
Last imported at : Nov. 19, 2023, noon
Source : ClinicalTrials.gov

Completed

Study design
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

nonRCT

Allocation
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Non-randomized

Design
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Single group assignment

Masking
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Open label

Center
Last imported at : March 15, 2023, 4 a.m.
Source : ClinicalTrials.gov

single-center

Study aim
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Prevention

Inclusion criteria
Last imported at : Nov. 16, 2021, 6:30 p.m.
Source : ClinicalTrials.gov

inclusion criteria: provision of signed and dated informed consent form stated willingness to comply with all study procedures and availability for the duration of the study male or female, aged 18 years of age or older previously diagnosed with mm/al amyloidosis (cohorts 1 or 3) or other hematologic malignancy (cohorts 2 or 3). previously received any one of the available covid-19 vaccines (between 4 and 36 weeks prior to enrollment) anti-sars-cov2 igg antibody titer of results less than 1.0 units (cohorts 1 and 2), or 1.0-1.99 units (cohort 3). antibody titers will be measured within 14 days of enrollment. if currently receiving potentially immunosuppressive anti-neoplastic therapy for their underlying hematologic condition, a two-week interruption in therapy before and after the booster dose of vaccine is encouraged but not required (physician discretion).-

Exclusion criteria
Last imported at : Nov. 16, 2021, 6:30 p.m.
Source : ClinicalTrials.gov

daily corticosteroids at a dose equivalent to prednisone 20 mg/day or greater during the period two weeks before enrollment to the trial. intermittent steroid dosing at or above this level is permitted (i.e., weekly dexamethasone dosing as part of myeloma therapy) history of previous severe reaction to any available covid-19 vaccine (defined as any grade 3 or higher reaction) febrile illness within 3 days of booster dosing. documented sars-cov2 infection within 2 weeks of enrollment. less than 3 months post-autologous or allogeneic stem cell transplant (note: transplant between initial standard vaccine administration and enrollment is not otherwise grounds for exclusion from participation).

Number of arms
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

1

Funding
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Barbara Ann Karmanos Cancer Institute

Inclusion age min
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

18

Inclusion age max
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

100

Countries
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

United States

Type of patients
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

High risk patients

Severity scale
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

N/A

Total sample size
Last imported at : Aug. 30, 2022, 9:30 p.m.
Source : ClinicalTrials.gov

119

primary outcome
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Observed response rate of anti-SARS-CoV2 antibody seroconversion.

Notes
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

None

Phase
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

Phase 2

Arms
Last imported at : Sept. 1, 2021, 8:30 p.m.
Source : ClinicalTrials.gov

[{"arm_notes": "one dose booster, previsouly vaccinated with any of the SARS-CoV2 vaccines authorized in the USA", "treatment_id": 824, "treatment_name": "Mrna-1273", "treatment_type": "Rna based vaccine", "pharmacological_treatment": "Vaccine"}]