Multiple MyelomaPhase 2NCT07489534
Study of PD-1Ab21-BCMA CAR-T Therapy for Consolidation of Multiple Myelomawith Renal Dysfunction
A Phase 2 study testing PD-1Ab21-BCMA CAR-T cell immunotherapy in people with Multiple Myeloma, run by Daihong Liu at 1 site in China.
Trial summary
The purpose of this study is to determine the efficacy and safety of targeted BCMA CART cells secreting PD1 and interleukin 21 fusion protein immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction. Read more about this study
- Who is it for?
- Ages 14 years and older
- Conditions the study is for
- Multiple Myeloma
- What is being tested?
- PD-1Ab21-BCMA CAR-T cell immunotherapy
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 25 participants
- Where
- 1 siteChina
- Study dates
- 29 Sep 2025to 31 Jul 2027
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Age: Over 14 years old
- Diagnosed with multiple myeloma accompanied by renal dysfunction, received ≥ 2 courses of clinical first-line treatment, evaluated efficacy above PR, and predicted survival of more than three months.
- The hospital examination meets the following indicators:
- ECOG physical status score 0-2 or KPS score>80 points
- Having sufficient venous access for single or intravenous blood collection, and no other blood cells Separation contraindications
- WBC≥1×109/L,LY≥0.3×109/L,
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- ALT and AST ≤ 2.5 ULN
- Serum total bilirubin ≤ 2.0mg/dL (34.2 μmol/L)
- PT:INR<1.7 or PT prolonged by<4s compared to normal value
Who cannot join
- Pregnant or lactating women (the safety of this treatment for unborn babies is unknown, and the assessment of pregnancy status for female participants is negative in serum or urine pregnancy tests within 48 hours prior to infusion);
- Any uncontrollable active infection;
- Presence of active hepatitis B or C virus infection;
- HIV/AIDS infection;
- Has neurological disorders;
- Within 2 weeks prior to signing the informed consent form, systemic use of steroid drugs (inhalable steroids may be used);
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- Allergies to immunotherapy and related drugs;
- Currently, there are patients with heart disease or poorly controlled hypertension who require treatment;
- Currently, patients with unstable or active ulcers or gastrointestinal bleeding;
- Patients with a history of organ transplantation or waiting for organ transplantation;
- Hyponatremia, blood sodium<125mmol/L;
- Baseline blood potassium<3.5mmol/L (potassium can be supplemented before participating in the study to restore blood potassium levels above this level);
- The patient needs anticoagulant therapy (such as warfarin or heparin);
- The patient requires long-term antiplatelet therapy (aspirin, dose>300mg/d); Clopidogrel, dose>75mg/d).
- Additionally,
- Patients currently participating in other clinical trials;
- Researchers believe that other reasons are not suitable for clinical trial participants.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site, 1 recruiting
- Recruiting
Chinese PLA General Hospital
Beijing, Beijing Municipality, 100853
About this study
Official title: Exploratory Clinical Study on PD-1Ab21-BCMA CAR-T Cells (CD203) for First-line Consolidation Therapy of Multiple Myeloma With Renal Dysfunction
The purpose of this study is to determine the efficacy and safety of targeted BCMA CART cells secreting PD1 and interleukin 21 fusion protein immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction.
Read the detailed description
Renal dysfunction is a poor prognostic factor for multiple myeloma(MM). Compared with MM patients with normal renal function, MM patients with renal dysfunction have significantly reduced median overall survival. The clinical outcomes of MM patients with improved renal function after treatment have shown some improvement, but are still inferior to those of MM patients with normal renal function. Although renal dysfunction is not an absolute contraindication for autologous hematopoietic stem cell transplantation, the therapeutic effect is unsatisfactory. For MM patients with renal insufficiency, the dosage of transplant pre-treatment drugs should be reduced according to creatinine clearance rate, and renal insufficiency increases the incidence of transplant related toxic side effects such as mucositis, infections, and other complications. In recent years, CART cell therapy has achieved good therapeutic effects in MM patients with renal dysfunction.Xuzhou Medical University Affiliated Hospital has reported 7 patients with refractory or recurrent MM accompanied by severe renal dysfunction. These patients were treated with CART cell therapy targeting BCMA or in combination targeting CD19/BCMA, with 5 cases achieving complete remission and 2 cases achieving partial remission. It is worth noting that the renal remission rate reached 100%. The results from Tongji Hospital in Wuhan show that CART can significantly improve renal function in relapsed and refractory MM patients. In multiple myeloma with renal dysfunction, BCMA CART cell consolidation therapy after first-line induction therapy may achieve rapid and lasting hematological and renal remission.
Numerous studies have confirmed that the anti-tumor effect of T cells depends on their proliferation ability. The therapeutic effect of PD-1 antibody depends on the recovery of CD8+T cell function with proliferative ability, while terminal failure CD8+T cells lacking proliferative ability do not respond to PD-1 antibody treatment. In clinical trials of T cell therapy for solid tumors, IL-2 should be administered simultaneously with T cell infusion to promote T cell proliferation. There are also many research reports on CAR-T cells expressing and secreting various cytokines both domestically and internationally. The T cell cytokine IL-2/15/21 is the most effective T cell response enhancer, but due to its numerous target cells, it has significant side effects. This greatly limits their clinical application. To this end, we have established an immunotherapy strategy that targets tumor specific T cells with cytokines. The developed anti-PD-1 antibody and IL-21 fusion protein (PD-1Ab21) not only exert the therapeutic effect of PD-1 antibody, but also target PD-1 positive tumor specific T cells in vivo with IL-21, promoting the formation of memory T cells and greatly improving the effectiveness of tumor treatment. Based on the above research, we developed BCMA CAR-T cells (PD-1Ab21-BCMA CAR-T) expressing PD-1 single chain antibody and IL-21 fusion protein (PD-1Ab21). The supernatant of CAR-T cell culture contains high-level PD-1Ab21 fusion protein that can bind to PD-1 on the cell surface, block anti-PD-1 signaling, and enrich IL-21 on the surface of CAR-T cells, binding to its receptor. In preclinical mouse tumor model experiments, it has been confirmed that the therapeutic effect of PD-1Ab21-BCMA CAR-T cells is significantly better than that of ordinary BCMA CAR-T cells. A clinical trial initiated by researchers for the treatment of refractory/recurrent MM was conducted at the First Medical Center of the General Hospital of the People's Liberation Army. Ten patients have been treated, with six achieving complete remission (CR), including one relapse and three VGPR, including three extramedullary lesions. There are also three cases yet to be evaluated, demonstrating good therapeutic efficacy and safety.
This study plans to explore the effectiveness and safety of PD-1Ab21-BCMA CAR-T cell immunotherapy as first-line consolidation therapy for multiple myeloma with renal dysfunction after first-line induction therapy, in order to improve the prognosis of such patients and provide new treatment options for first-line consolidation therapy of multiple myeloma with renal dysfunction.
- Conditions
- Multiple Myeloma
- Being tested
- PD-1Ab21-BCMA CAR-T cell immunotherapy
- Keywords
- multiple myeloma; renal dysfunction; CART; fusion protein; consolidation therapy
- Medical subject headings
- Multiple Myeloma, Renal Insufficiency
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PD-1Ab21-BCMA CAR-T cell immunotherapyDrug
Consolidation therapy with PD-1 antibody and BCMA-targeting CAR-T in multiple myeloma patients with renal impairment.
| Study group | Role | What they receive |
|---|---|---|
| multiple myeloma patients with renal dysfunction who accept PD- 1Ab21-BCMA CAR-T cell immunotherapy | Experimental | Not described Receives: Drug: PD-1Ab21-BCMA CAR-T cell immunotherapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
1-year progression free survival rate (1-year-PFS)
The 1-year progression free survival rate (1-year-PFSR) of PD-1Ab21-BCMA CAR-T cell immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction refers to the proportion of disease progression that occurs within one year after treatment in patients.
Measured: 1 year after treatment
Secondary outcomes (8)
overall survival (OS)
Overall survival (OS) refers to the time from the start of treatment to the death of the patient for any reason.
Measured: 2 years after treatment
progression free survival (PFS)
Progression free survival (PFS) refers to the time from treatment to the first myeloma progression or death of the patient for any reason.
Measured: 2 years after treatment
time to progression (TTP)
Time to progression (TTP) refers to the time from treatment to the first myeloma progression.
Measured: 2 years after treatment
disease free survival (DFS)
Disease free survival (DFS) refers to the time from treatment to the first myeloma recurrence.
Measured: 2 years after treatment
duration of response (DOR)
Duration of Response (DOR) refers to the time from the first assessment of a myeloma as a complete or partial response to the first assessment of PD (Progressive Disease) or death from any cause.
Measured: 2 years after treatment
event free survival (EFS)
Event Free Survival (EFS) is a commonly used endpoint indicator in clinical trials to evaluate the survival time of patients without any adverse events during a specific time period. These adverse events include but are not limited to disease progression, death, treatment plan changes, and the occurrence of serious side effects.
Measured: 2 years after treatment
recurrence rate
The recurrence rate refers to the proportion of patients with lymphoma recurrence after treatment.
Measured: 2 years after treatment
safety
The safety of this PD-1Ab21-BCMA CAR-T immunotherapy.
Measured: 2 years after treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Mar 2026
- Study start29 Sep 2025
- Primary completion31 Jul 2027 (estimated)
- Study completion31 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Multiple MyelomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 25 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Daihong Liu
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Daihong Liu, Chinese PLA General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07489534
- Sponsor's protocol ID
- S2025-670-01
- Status last verified
- Oct 2025
- First submitted
- 18 Mar 2026
- Last updated
- 24 Mar 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Exploratory Clinical Study on PD-1Ab21-BCMA CAR-T Cells (CD203) for First-line Consolidation Therapy of Multiple Myeloma With Renal Dysfunction
- ClinicalTrials.gov ID
- NCT07489534
- Acronym / sponsor ID
- S2025-670-01
- Conditions
- Multiple Myeloma
- Keywords
- multiple myeloma; renal dysfunction; CART; fusion protein; consolidation therapy
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 25 participants (estimated)
- Lead sponsor
- Daihong LiuUniversity, hospital or other
- Study start
- 29 Sep 2025 (actual)
- Primary completion
- 31 Jul 2027 (estimated)
- Study completion
- 31 Jul 2027 (estimated)
- First posted
- 24 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine the efficacy and safety of targeted BCMA CART cells secreting PD1 and interleukin 21 fusion protein immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction.
Detailed description
Renal dysfunction is a poor prognostic factor for multiple myeloma(MM). Compared with MM patients with normal renal function, MM patients with renal dysfunction have significantly reduced median overall survival. The clinical outcomes of MM patients with improved renal function after treatment have shown some improvement, but are still inferior to those of MM patients with normal renal function. Although renal dysfunction is not an absolute contraindication for autologous hematopoietic stem cell transplantation, the therapeutic effect is unsatisfactory. For MM patients with renal insufficiency, the dosage of transplant pre-treatment drugs should be reduced according to creatinine clearance rate, and renal insufficiency increases the incidence of transplant related toxic side effects such as mucositis, infections, and other complications. In recent years, CART cell therapy has achieved good therapeutic effects in MM patients with renal dysfunction.Xuzhou Medical University Affiliated Hospital has reported 7 patients with refractory or recurrent MM accompanied by severe renal dysfunction. These patients were treated with CART cell therapy targeting BCMA or in combination targeting CD19/BCMA, with 5 cases achieving complete remission and 2 cases achieving partial remission. It is worth noting that the renal remission rate reached 100%. The results from Tongji Hospital in Wuhan show that CART can significantly improve renal function in relapsed and refractory MM patients. In multiple myeloma with renal dysfunction, BCMA CART cell consolidation therapy after first-line induction therapy may achieve rapid and lasting hematological and renal remission.
Numerous studies have confirmed that the anti-tumor effect of T cells depends on their proliferation ability. The therapeutic effect of PD-1 antibody depends on the recovery of CD8+T cell function with proliferative ability, while terminal failure CD8+T cells lacking proliferative ability do not respond to PD-1 antibody treatment. In clinical trials of T cell therapy for solid tumors, IL-2 should be administered simultaneously with T cell infusion to promote T cell proliferation. There are also many research reports on CAR-T cells expressing and secreting various cytokines both domestically and internationally. The T cell cytokine IL-2/15/21 is the most effective T cell response enhancer, but due to its numerous target cells, it has significant side effects. This greatly limits their clinical application. To this end, we have established an immunotherapy strategy that targets tumor specific T cells with cytokines. The developed anti-PD-1 antibody and IL-21 fusion protein (PD-1Ab21) not only exert the therapeutic effect of PD-1 antibody, but also target PD-1 positive tumor specific T cells in vivo with IL-21, promoting the formation of memory T cells and greatly improving the effectiveness of tumor treatment. Based on the above research, we developed BCMA CAR-T cells (PD-1Ab21-BCMA CAR-T) expressing PD-1 single chain antibody and IL-21 fusion protein (PD-1Ab21). The supernatant of CAR-T cell culture contains high-level PD-1Ab21 fusion protein that can bind to PD-1 on the cell surface, block anti-PD-1 signaling, and enrich IL-21 on the surface of CAR-T cells, binding to its receptor. In preclinical mouse tumor model experiments, it has been confirmed that the therapeutic effect of PD-1Ab21-BCMA CAR-T cells is significantly better than that of ordinary BCMA CAR-T cells. A clinical trial initiated by researchers for the treatment of refractory/recurrent MM was conducted at the First Medical Center of the General Hospital of the People's Liberation Army. Ten patients have been treated, with six achieving complete remission (CR), including one relapse and three VGPR, including three extramedullary lesions. There are also three cases yet to be evaluated, demonstrating good therapeutic efficacy and safety.
This study plans to explore the effectiveness and safety of PD-1Ab21-BCMA CAR-T cell immunotherapy as first-line consolidation therapy for multiple myeloma with renal dysfunction after first-line induction therapy, in order to improve the prognosis of such patients and provide new treatment options for first-line consolidation therapy of multiple myeloma with renal dysfunction.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| multiple myeloma patients with renal dysfunction who accept PD- 1Ab21-BCMA CAR-T cell immunotherapy | Experimental | Drug: PD-1Ab21-BCMA CAR-T cell immunotherapy |
Who may qualify
- Ages
- 14 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (9 listed)
- Age: Over 14 years old
- Diagnosed with multiple myeloma accompanied by renal dysfunction, received ≥ 2 courses of clinical first-line treatment, evaluated efficacy above PR, and predicted survival of more than three months.
- The hospital examination meets the following indicators:
Key exclusion criteria (17 listed)
- Pregnant or lactating women (the safety of this treatment for unborn babies is unknown, and the assessment of pregnancy status for female participants is negative in serum or urine pregnancy tests within 48 hours prior to infusion);
- Any uncontrollable active infection;
- Presence of active hepatitis B or C virus infection;
- HIV/AIDS infection;
- Has neurological disorders;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PD-1Ab21-BCMA CAR-T cell immunotherapyConsolidation therapy with PD-1 antibody and BCMA-targeting CAR-T in multiple myeloma patients with renal impairment. | Drug | multiple myeloma patients with renal dysfunction who accept PD- 1Ab21-BCMA CAR-T cell immunotherapy |
Primary outcome
1-year progression free survival rate (1-year-PFS)
Time frame: 1 year after treatment
The 1-year progression free survival rate (1-year-PFSR) of PD-1Ab21-BCMA CAR-T cell immunotherapy for first-line consolidation therapy of multiple myeloma with renal dysfunction refers to the proportion of disease progression that occurs within one year after treatment in patients.
8 secondary outcomes
overall survival (OS)
Time frame: 2 years after treatment
progression free survival (PFS)
Time frame: 2 years after treatment
time to progression (TTP)
Time frame: 2 years after treatment
disease free survival (DFS)
Time frame: 2 years after treatment
duration of response (DOR)
Time frame: 2 years after treatment
event free survival (EFS)
Time frame: 2 years after treatment
recurrence rate
Time frame: 2 years after treatment
safety
Time frame: 2 years after treatment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Mar 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing PD-1Ab21-BCMA CAR-T cell immunotherapy in people with Multiple Myeloma, run by Daihong Liu at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 24 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Li-Ping Dou, Dr. (86-010-66937232, lipingruirui@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
1-year progression free survival rate (1-year-PFS) (time frame: 1 year after treatment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Mar 2026.