Viewing Study NCT06248086



Ignite Creation Date: 2024-05-06 @ 8:04 PM
Last Modification Date: 2024-10-26 @ 3:20 PM
Study NCT ID: NCT06248086
Status: RECRUITING
Last Update Posted: 2024-06-28
First Post: 2024-01-31

Brief Title: A Study to Find a Suitable Dose of ASP2802 in People With CD20-positive B-cell Lymphomas
Sponsor: Astellas Pharma Global Development Inc
Organization: Astellas Pharma Inc

Study Overview

Official Title: A First-in-Human Phase 1 Study to Assess the Safety Pharmacokinetics Pharmacodynamics and Preliminary Efficacy of a Single-Induction Dose of convertibleCARTM-T Cells Armed With MicAbodyTM Protein ASP2802 Followed by Maintenance Booster Doses of the MicAbody Protein in Patients With CD20-Positive Relapsed or Refractory B-Cell Lymphomas
Status: RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: CAR-T cell therapy is a type of treatment for people with certain lymphomas T-cells are white blood cells that help to fight infections CAR-T cell therapy improves the bodys T-cells to help them better fight cancer cells

ASP2802 is a type of CAR-T cell therapy given with MA-20 MA-20 is a protein that helps the CAR-T cell therapy work inside the body

Before ASP2802 is available as a treatment the researchers need to understand how it is processed by and acts upon the body This information will help find a suitable dose for future studies and check for potential medical problems from the treatment

In this study ASP2802 is being tested in humans for the first time ASP2802 has already been tested in the laboratory and in animals This is the standard way new potential treatments are developed

People taking part in this study will be adults with CD20-positive B-cell lymphomas CD20 is a protein found on a type of white blood cell called a B-cell Some people with B-cell lymphomas have more CD20 on these cells Their cancer will have come back after it had disappeared with earlier therapy relapsed or it will have become resistant to previous treatment refractory

The main aims of the study are to check the safety of ASP2802 how well it is tolerated and to find a suitable dose of ASP2802

This is an open-label adaptive study Open-label means that people in this study and clinic staff will know that people will receive ASP2802 treatment Adaptive means the treatments may change depending on earlier results in the study

There will be 3 groups of people in this study and 3 doses of ASP2802 Groups A B and C will receive ASP2802 treatment Group A will start treatment first with a low dose of ASP2802 If Group A tolerates the low dose of ASP2802 then Group B will receive the higher dose of ASP2802 If Group B tolerates the higher dose of ASP2802 then Group C will receive the highest dose of ASP2802

There are several steps in this treatment First T-cells are removed from the blood by inserting a small tube cannula into a vein and connecting it to a machine that separates out the blood cells The machine collects the T-cells and returns the rest of the blood cells back into the bloodstream The collected T-cells are sent to the lab to be changed into improved T-cells with ASP2802 to fight the cancer This may take several weeks so people in the study may receive extra treatment to keep the cancer under control during this time

Before the improved T-cells go back in the body people will visit the clinic so that the study doctors can do a series of checks to make sure they are well enough to receive the T-cells A few days before the improved T-cells go back into the body people in the study will have chemotherapy for 3 days This is to make sure the cancer is at its lowest level before people are treated with ASP2802 Then the improved T-cells are fed back into the bloodstream using a drip attached to the cannula After this a booster of MA-20 will be given at the set dose by infusion on Day 3 and Day 17 in a 28-day cycle If people respond well to treatment they may stay on the same dose during the next cycle if they have medical problems from the treatment they may get a lower dose during the next cycle The next group of people may receive a different dose higher or lower of MA-20 depending on the results from the previous group People in the study will continue receiving MA-20 in this way until they have certain medical problems from the treatment on the lowest dose of MA-20 they start other cancer treatment their cancer gets worse they or the study doctor decides they should stop treatment they do not come back for treatment

After treatment has finished people in the study will visit the clinic regularly for 2 years and continue to be monitored for up to 15 years

Some people may be treated again with MA-20 This may happen for people who have responded to treatment and then relapse within a year or for people that have a partial response and have a slow growing lymphoma

During the study people will visit the study hospital many times During most visits the study doctors will do a medical examination blood tests and check vital signs Vital signs include temperature breathing rate blood pressure blood oxygen levels and heart rate They will also check for medical problems In some visits computerized tomography CT scans and electrocardiograms ECGs to check the heart rhythm will also be done

People will have several hospital stays during their treatment This may be during their chemotherapy then from Days -1 to 7 and Days 17 to 21 during the cycle 1 of MA-20 Day -1 means 1 day before treatment with ASP2802 During this time people will be closely monitored for medical problems have EGCs and have a biopsy taken During the extra cycles of MA-20 there will be the option of staying overnight
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None