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P-CD19CD20-ALLO1

Phase 1

Diffuse Large B-Cell Lymphoma, Not Otherwise Specified | Monoclonal antibody | Oncology |cbdMD, Inc.|Last Updated: May 7, 2026

Success Probability

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Market & Valuation

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Trial Design

CONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment120

FDA Designations

No designations recorded

Clinical trial landscape

P-CD19CD20-ALLO1 · 1 trial · 10 indications

Phase 1 1
NCT06014762P-CD19CD20-ALLO1 Allogeneic CAR-T Cells in the Treatment of Subjects With B Cell MalignanciesDiffuse Large B-Cell Lymphoma, Not Otherwise Specified
ACTIVE NOT_RECRUITING120 Analytics
PHASE1ACTIVE NOT_RECRUITING
P-CD19CD20-ALLO1 Allogeneic CAR-T Cells in the Treatment of Subjects With B Cell Malignancies
Diffuse Large B-Cell Lymphoma, Not Otherwise SpecifiedUnlock trial analytics

Study Endpoints

Primary Endpoints

Assess the safety and MTD or RDE of P-CD19CD20-ALLO1 based on dose limiting toxicities (DLT)
Baseline through 28 days

Rate of DLT's

Secondary Endpoints

The safety of P-CD19CD20-ALLO1 (AEs)
Baseline through 36 months
The anti-B cell malignancy effect of P-CD19CD20-ALLO1 (ORR)
Baseline through 15 years
The anti-B cell malignancy effect of P-CD19CD20-ALLO1 (DOR)
Baseline through 15 years
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
P-CD19CD20-ALLO1 CAR-T Cells (Arm S)EXPERIMENTALP-CD19CD20-ALLO1 following conditioning chemotherapy regimen S. Rimiducid may be administered.
P-CD19CD20-ALLO1 CAR-T Cells (Arm LD 750)EXPERIMENTALP-CD19CD20-ALLO1 following conditioning chemotherapy regimen LD 750. Rimiducid may be administered.
P-CD19CD20-ALLO1 CAR-T Cells (Arm LD 1000)EXPERIMENTALP-CD19CD20-ALLO1 following conditioning chemotherapy regimen LD 1000. Rimiducid may be administered.

Interventions

NameTypeDescription
P-CD19CD20-ALLO1BIOLOGICALSingle weight-based IV administration
RimiducidDRUGSingle weight-based IV administration
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites16

Inclusion Criteria 1. Must have signed written, informed consent. 2. Males or females ≥ 18 years of age. 3. Must have prior biopsy proven confirmed diagnosis of DLBCL NOS (including DLBCL arising from indolent lymphomas), HGBL, PMBCL,and tFL or follicular lymphoma Grade 3B. 4. Diagnosis of the dise...

Countries:United States
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Frequently asked questions about P-CD19CD20-ALLO1

What is P-CD19CD20-ALLO1 used for?

P-CD19CD20-ALLO1 is an investigational allogeneic CAR-T cell therapy being studied for the treatment of B cell malignancies, including Diffuse Large B-Cell Lymphoma, Not Otherwise Specified, High-grade B-cell Lymphoma, Primary Mediastinal Large B-cell Lymphoma, Transformed Follicular Lymphoma, and Follicular Lymphoma Grade 3B. It is currently in Phase 1 clinical development.

Who is developing P-CD19CD20-ALLO1?

P-CD19CD20-ALLO1 is being developed by cbdMD, Inc., a company traded on the stock exchange under the ticker symbol YCBD. The therapy is an allogeneic CAR-T cell product being evaluated in oncology, specifically for B cell malignancies.

What phase is P-CD19CD20-ALLO1 in?

P-CD19CD20-ALLO1 is in Phase 1 clinical development. It is an investigational therapy, meaning it has not been approved by regulatory authorities and is still being studied in clinical trials to assess its safety and efficacy in patients with B cell malignancies.

What clinical trials is P-CD19CD20-ALLO1 in?

P-CD19CD20-ALLO1 is being studied in a Phase 1 clinical trial with the identifier NCT06014762. The trial is titled 'P-CD19CD20-ALLO1 Allogeneic CAR-T Cells in the Treatment of Subjects With B Cell Malignancies' and is active but not recruiting participants. The study is enrolling up to 120 participants in the United States.

Is P-CD19CD20-ALLO1 a monoclonal antibody?

P-CD19CD20-ALLO1 is classified as a monoclonal antibody modality, but it is specifically an allogeneic CAR-T cell therapy. This means it involves genetically engineered T cells from a donor that are designed to target CD19 and CD20 antigens on B cells. It is being developed for the treatment of B cell malignancies.