A Clinical Study of of RN1701 Injection in the Treatment of Relapsed/Refractory B-Cell Lymphomas

YANRU WANG

Status and phase

Not yet enrolling

Phase 1

Conditions

Relapsed/Refractory B-cell Lymphoma

Treatments

Biological: RN1701 injection

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT07316920

RN1701JB

Details and patient eligibility

About

This single-arm, open-label pilot study will assess the safety and efficacy of RN1701, a bispecific CD19/CD20-targeted allogeneic CAR-T-cell product, in patients with relapsed or refractory B-cell lymphoma. Up to 19 participants will be enrolled in a conventional 3 + 3 dose-escalation scheme. The primary objective of the study is to evaluate the safety and feasibility of RN1701 for the treatment of relapsed/refractory B-cell lymphoma. The secondary objective is to evaluate the efficacy of RN1701 for the treatment of relapsed/refractory B-cell lymphoma. The exploratory objective is to evaluate the expansion, persistence, and ability of RN1701 to deplete CD19- and/or CD20-positive cells in patients with relapsed/refractory B-cell lymphoma.

Enrollment

19 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Voluntary participation; full understanding of the study and provision of written informed consent obtained before any study-related procedure not part of standard care; willingness to comply with follow-up.
Age 18-75 years; either sex.
ECOG performance status 0-1.
Histologically confirmed large B-cell lymphoma, follicular lymphoma, mantle-cell lymphoma, or indolent lymphoma transformed to DLBCL; CD19 and/or CD20 positive.
At least one measurable lesion per Lugano criteria: nodal lesion longest diameter >1.5 cm, extranodal lesion >1.0 cm.
Prior treatment response must meet one of the following:

• Large B-cell lymphoma, grade 3B follicular lymphoma, transformed indolent lymphoma: i. Primary refractory and ineligible/unable to receive autologous CAR-T: best response PD after ≥2 cycles of first-line therapy, or SD after ≥4 cycles.

ii. Relapse ≤12 months after achieving CR with first-line chemo-immunotherapy. iii. Relapse/progression ≤12 months after autologous HSCT. iv. Refractory to, relapsed after, or progressed on ≥2 prior lines (including autologous CAR-T): best response PD or SD after ≥2 cycles of the most recent regimen.

v. Transformed indolent lymphoma: prior chemotherapy for iNHL and ≥1 systemic regimen after transformation, fulfilling the above refractory/relapse criteria.

• Grade 1, 2, or 3A follicular lymphoma: i. Primary refractory and ineligible/unable to receive autologous CAR-T: best response PD after ≥2 cycles of first-line therapy.

ii. Refractory to, relapsed after, or progressed on ≥2 prior lines (including autologous CAR-T): best response PD or SD after ≥2 cycles of the most recent regimen.

• Mantle-cell lymphoma: i. Primary refractory and ineligible/unable to receive autologous CAR-T: best response PD after ≥2 cycles of first-line therapy, or SD after ≥4 cycles.

ii. Refractory to, relapsed after, or progressed on ≥2 prior lines (including autologous CAR-T): best response PD or SD after ≥2 cycles of the most recent regimen.
Estimated life expectancy ≥3 months.
Screening laboratory values (may be repeated once):
- Hemoglobin ≥8.0 g/dL (no transfusion within 7 days).
- Platelets ≥50×10⁹/L (no transfusion within 7 days).
- ANC ≥1.0×10⁹/L (growth-factor support allowed if none within 7 days of test).
- AST/ALT ≤3×ULN (≤5×ULN if liver involvement).
- Serum creatinine ≤1.5×ULN or CrCl ≥60 mL/min (Cockcroft-Gault).
- Total bilirubin ≤2×ULN (≤3×ULN if liver involvement); except congenital bilirubin disorders (e.g., Gilbert's syndrome: direct bilirubin ≤1.5×ULN).
- INR, PT, APTT <1.5×ULN.
Toxicities from prior anti-cancer therapy (except alopecia, nausea, and the above lab values) must have stabilized at baseline or resolved to ≤Grade 1.
WOCBP must have a negative high-sensitivity serum β-hCG pregnancy test at screening and again before the first dose of cyclophosphamide/fludarabine.
Subjects of reproductive potential must use effective contraception for ≥12 months after completing study therapy.

Exclusion criteria

Subjects with any of the following conditions are ineligible for this trial:
1. Any malignancy other than B-cell non-Hodgkin lymphoma ever diagnosed or treated, except:
  - Malignancy that received curative therapy and has shown no evidence of active disease for ≥2 years before enrolment; or
  - Adequately treated non-melanoma skin cancer with no current evidence of disease.
2. Prior anti-cancer therapy within the stated windows (before lymphodepletion):
  - CNS prophylaxis (e.g., intrathecal methotrexate and/or cytarabine) within 7 days;
  - Cytotoxic chemotherapy or radiotherapy within 14 days;
  - Small-molecule targeted or epigenetic therapy within 14 days or 5 half-lives, whichever is longer;
  - Monoclonal antibody, bispecific antibody, or antibody-drug conjugate within 21 days or 5 half-lives, whichever is shorter;
  - Investigational drug or invasive investigational device within 28 days (if the therapy is also investigational, the 28-day wash-out applies);
  - Autologous haematopoietic stem-cell transplant or CD19-directed autologous CAR-T therapy within 100 days.
3. Any autologous cellular or gene therapy other than CD19-directed autologous CAR-T.
4. Any allogeneic cellular (including CAR-T) or gene therapy.
5. Prior allogeneic haematopoietic stem-cell transplantation.
6. Positive donor-specific antibody (DSA).
7. At least one of the following high-risk features:
  - Sum of the product of perpendicular diameters (SPD) of all measurable lesions ≥100 cm²;
  - Bulky disease: single mass ≥7.5 cm; mediastinal mass with maximum diameter >1/3 of thoracic diameter;
  - Obstructive/compressive emergency (e.g., bowel obstruction, vascular compression) requiring urgent intervention at screening.
8. Active CNS involvement (symptomatic or positive CSF/imaging); subjects with prior CNS disease now in remission (asymptomatic with negative CSF and imaging) are eligible.
9. Significant bleeding diathesis: gastrointestinal bleeding, haemorrhagic cystitis, coagulopathy, hypersplenism (splenomegaly on exam/US, cytopenias, hyperplastic marrow) or ongoing anticoagulation.
10. Chronic concomitant systemic corticosteroids or other immunosuppressants, except: topical, ocular, intra-articular, nasal or inhaled corticosteroids; short-course steroids for prophylaxis (e.g., contrast allergy).
11. Severe underlying medical conditions:
  - Active serious viral, bacterial or uncontrolled systemic fungal infection;
  - Active systemic autoimmune disease requiring therapy.
12. Significant cardiac disease:
  - NYHA class III or IV congestive heart failure;
  - Myocardial infarction or CABG within 6 months before enrolment;
  - Clinically relevant ventricular arrhythmia or unexplained syncope not vasovagal or dehydration-related;
  - Severe non-ischaemic cardiomyopathy;
  - Left ventricular ejection fraction (LVEF) <45% by echo or MUGA within 4 weeks before lymphodepletion.
13. Resting oxygen saturation <92%.
14. Clinically relevant prior or current CNS disorder: epilepsy, seizure-like episodes, paralysis, aphasia, stroke, severe head trauma, dementia, Parkinson's disease, cerebellar disorder, organic brain syndrome or major psychiatric illness.
15. Live-attenuated vaccine within 4 weeks before screening.
16. Major surgery within 2 weeks before screening or planned within 2 weeks after study treatment (local anaesthesia allowed).
17. Positive screen for HBsAg, HBeAg, HBV DNA, HCV antibody, HCV RNA, or HIV antibody.
18. Life-threatening allergy, hypersensitivity or intolerance to study-drug excipients including, but not limited to, DMSO.
19. Lactating women.
20. Any condition that, in the investigator's opinion, renders the subject unsuitable for the study.