Clinical trial · Interventional
A Study of TQB3820 in Patients With Hematological Malignancies
A Phase I Study to Evaluate the Tolerability and Pharmacokinetics of TQB3820 in Relapsed or Refractory Multiple Myeloma (R/R MM) or Relapsed or Refractory Indolent B-cell Non-Hodgkin's Lymphoma (R/R B-NHL)
NCT05020639CI-TRIAL-00053989unknownPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
TQB3820 is a novel cereblon-modulating agent. Upon binding to cereblon, a substrate receptor in the cullin4 E3 ligase complex, TQB3820 promotes recruitment, ubiquitination, and subsequent proteasomal degradation of the hematopoietic transcription factors Ikaros (IKZF1) and Aiolos (IKZF3). Modulation of Aiolos and Ikaros expression has the potential to correct multiple aspects of the immune dysregulation mediated by B cells.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hematological Malignancies | Hematopoietic and Lymphoid Cell Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| TQB3820 tablets | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- TQB3820 tablets
- description
- TQB3820 tablets are administrated orally on Days 1-28 of each 28-day treatment cycle. Dose escalation of TQB3820 will be based on evaluation of clinical safety and tolerability and guided by accumulating PK data.
- interventionNames
- Drug: TQB3820 tablets
Primary outcomes (4)
- measure
- Dose-limiting toxicity (DLT)
- timeFrame
- up to 18 months
- description
- DLT describes side effects of a drug or other treatment that are serious enough to prevent an increase in dose or level of that treatment.
- measure
- Maximum Tolerated Dose (MTD)
- timeFrame
- up to 18 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria:
1. For Multiple Myeloma cohort
1. Patients must have received at least 2 prior therapies;
2. Measurable levels of myeloma paraprotein
1. M-protein in serum \>5 g/L;
2. M-protein in urine \>200mg/24h;
3. Light chain Multiple Myeloma without measurable disease in the serum or urine: serum immunoglobulin free light chain ≥ 100 mg/L and abnormal serum immunoglobulin kappa lambda free light chain ratio.
2. For Indolent B-NHL
1. Progressed after standard treatment or no standard treatment with an established survival benefit is available;
2. Imaging in screening showing at least one measurable lesion; In patients with CLL/SLL, circulating lymphocytes \>= 5.0 × 10\^9/L or lesions greater than 1.5 cm.
3. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2;
4. Life expectancy \>=3 months;
5. Adequate organ/system function;
6. Female patients of childbearing age should agree to use contraceptive measures during the study period and for at least 6 months after study is stopped; male patients should agree to use contraception during the study period and for at least 6 months after study is stopped;
Exclusion Criteria:
1. Patients received allogenic haemopoietic stem cell transplantation, or autologous stem cell transplantation within 3 months;
2. Diagnosed and/or treated additional malignancy within 3 years before the first dose;
3. With factors affecting oral medication;
4. Toxicity that is \>=Grade 2 caused by previous cancer therapy;
5. Patients with congenital bleeding or coagulopathy, or are being treated with anticoagulants;
6. Patients with uncontrolled infections;
7. Has received surgery, chemotherapy, radiotherapy or other anticancer therapies 2 weeks before the first dose;
8. Has received Chinese patent medicines with anti-tumor indications that National Medical Products Administration(NMPA) approved within 2 weeks before the first dose;
9. Pleural effusion, pericardial effusion or ascites that cannot be controlled and need repeated drainage;
10. Central nervous system metastases;
11. Has participated in other clinical studies within 4 weeks before the first dose;
12. According to the judgement of the researchers, there are other factors that subjects are not suitable for the study.References
Publications (0)
Data not yet available
No reference posted for this study.