Viewing Protocol Section

Home Icon Home Search Icon Search Alerts Icon Stocks Certify Doc Icon Certify Doc Certify Doc Icon Genes Certify Doc Icon Clinical Trials Certify Doc Icon CompTox Processes Icon DrugMatrix Open Targets Icon Open Targets Processes Icon Products Support Icon Support Bugs Icon Bugs eRecord Icon eRecord
Main Search All Studies All Organizations Report Bug
Viewing Protocol Section

Thank You for evaluating our software.

Clinical Trials

To give you an idea of how we make custom software. We have taken all of the Clinical Trials Information from our Federal Government(https://clinicaltrials.gov/).

The JSON File Structure of the files is as follows: Full Study -> Study => Sections => Modules. You are currently viewing a Protocol Section and its Modules.

We give the table structure here to give you an idea of what you are looking at. We put the explanation to the left and the data to the right.

A Protocol Section has the following Modules.

1. Identification Module

2. Status Module

3. Sponsor Collaborators Module

4. Oversight Module

5. Description Module

6. Conditions Module

7. Design Module

8. Arms Interventions Module

9. Outcomes Module

10. Eligibility Module

11. Contacts Locations Module

12. References Module

13. IPD Sharing Statement Module

Viewing Protocol Section

Study NCT06362044
Ignite Creation Date: 2024-05-06 @ 8:23 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06362044
Protocol Section: NCT06362044
Start Identification Module Data
Expand Identification Module Data
Brief Title: A Study to Assess Frequency of Undetectable Minimal Residual Disease uMRD in Adult Participants With Chronic Lymphocytic Leukemia CLL Receiving Oral Venetoclax Tablets Intravenously IV Infused Rituximab in Routine Clinical Practice in Japan
Official Title: The Frequency of uMRD in Japanese Patients With CLL After 24 Months of Treatment With VenetoclaxRituximab in the 2L in the Real-World Setting
Acronym: None
Organization: AbbVie
Organization Class: INDUSTRY
Organization Study ID: P24-120
Start Status Module Data
Status Verified Date: 2024-04
Overall Status: RECRUITING
Study First Submit Date:
Study First Submit QC Date:
Last Update Submit Date:
Status:
Start Sponsor Collaborators Module Data
Investigator:
Lead Sponsor: AbbVie
Lead Sponsor Class: INDUSTRY
Lead Sponsor: AbbVie
Start Oversight Module Data
Description Module:
Study Last Update Post Date Type(Status Module):
Attachment: Upload