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Recruiting Phase 2

Telitacicept for the Treatment of Connective Tissue Disease-associated Thrombocytopenia

NCT05998759 · tracked via the Priya Life Science China tracker
Phase
Phase 2
Started
2023-12-02
Last updated
2025-05-06

Condition(s) studied

Connective Tissue DiseasesThrombocytopenia

Investigational drug(s) / intervention(s)

Telitacicept →Placebo

Telitacicept: subcutaneous telitacicept 160 mg weekly for 24 weeks.

Placebo: subcutaneous placebo weekly for 24 weeks.

Study summary

The goal of this clinical trial is to evaluate the efficacy and safety of Telitacicept for the treatment of connective tissue disease-associated thrombocytopenia.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Subjects who have been diagnosed with connective tissue disease (CTD)-associated thrombocytopenia. And CTD includes primary Sjögren syndrome (according to the 2002 American College of Rheumatology (ACR)/ European League against Rheumatism (EULAR) classification criteria), systemic lupus erythematosus (SLE, according to the 1997 or the 2009 ACR classification criteria), and undifferentiated connective tissue disease (according to the 1999 international classification criteria) * Refractory thrombocytopenia defined as: Either: Failure to maintain sustained remission after treatment by glucocorticoid and at least one immunosuppressant (i.e. cyclophosphamide, cyclosporine, mycophenolate mofetil, azathioprine, tacrolimus, methotrexate, leflunomide and hydroxychloroquine, et al.) Or: Relapse during oral glucocorticoid tapering or after withdrawal * 50×10\^9/L\>PLT * anti-nuclear antibody (ANA) positive (≥1:80, any karyotype) detected in the laboratory of each research center * Standard therapy should be maintained stable for at least 14 days prior to the first dose of the experimental drug or placebo. Standard therapy refers to the following treatment (monotherapy or in combination): glucocorticoid, hydroxychloroquine, and other immunosuppressants (i.e. cyclophosphamide, cyclosporine, mycophenolate mofetil, azathioprine, tacrolimus, methotrexate and leflunomide, et al.) * Signed informed consent form, willing or able to participate in all required study evaluations and procedures Exclusion Criteria: * Vital organ lethal bleeding (including but not limited to central nervous system bleeding, digestive tract bleeding) at screening, or intracranial bleeding 6 months prior to screening * Antiphospholipid syndrome, thrombotic thrombocytopenia purpura, hemolytic uremic syndrome, or thrombocytopenia secondary to other causes (such as sepsis, Epstein-Barr virus infection, cytomegalovirus infection, Corona Virus Disease-19 (COVID-19) infection, drugs, etc.) * Hematopoietic system disorders, such as myelodysplastic syndrome, paroxysmal sleep hemoglobinuria, aplastic anemia, leukemia, lymphoma, myelofibrosis and so on * Severe cardiovascular system disease, including: unstable or uncontrollable disease or condition affecting the function of the heart (such as angina pectoris, congestive heart failure, uncontrolled hypertension or arrhythmia) * Arteriovenous thromboembolism events * Receiving antiplatelet or anticoagulant therapy at screening * Clinically significant electrocardiogram changes * corrected Q-T interval (QTc)\>450ms for male, QTc\>470ms for female * Severe pulmonary disease, including: unstable or uncontrollable disease or condition affecting respiratory function \[e.g., diffuse alveolar hemorrhage, severe pulmonary hypertension, severe pulmonary interstitial disease (peripheral blood oxygen saturation \<92% at rest without oxygen, or forced vital capacity (FVC)\<50%, or carbon monoxide diffusing capacity (DLCO)\<50%)\] * Severe kidney disease, including: severe lupus nephritis (urinary protein \> 6 g/24 hours or endogenous creatinine clearance \< 30 ml /min) 8 weeks prior to randomization, active nephritis requiring current protocol disallowed drugs, severe renal insufficiency requiring hemodialysis or prednisone ≥100mg/ day (or equivalent) for ≥14 days * SLE or non-SLE related central nervous system disease (including epilepsy, psychosis, organic encephalopathy syndrome, cerebrovascular accident, encephalitis, central nervous system vasculitis) 8 weeks prior to randomization * Active hepatitis, a history of severe liver disease. Subjects positive for hepatitis B surface antigen (HBsAg) or antibodies to hepatitis C virus are excluded. As for subjects with antibodies to hepatitis B core antigen (HBcAb), further hepatitis B virus (HBV)-DNA should be tested. If HBV-DNA is negative, subjects could be enrolled; otherwise, subjects should be excluded * Abnormal laboratory results (including but not limited to: alanine aminotransferase (ALT) or aspertate aminotransferase (AST)≥3×ULN (upper limit of normal), white blood cell count \<1.5×10\^9/L) * Subjects with known active infections (e.g., shingles, COVID-19, HIV, active tuberculosis, etc.), and active or recurrent gastrointestinal ulcers * Pregnant or lactating women, and subjects with a during plan during the trial * Allergic reaction: history of allergic reactions to human biological products * Treatment with B cell-targeting agents such as Rituximab or Epratuzumab or Belimumab six months prior to randomization * Treatment with tumor necrosis factor (TNF) inhibitors or TNF-receptor blockers six months prior to randomization * Participating in clinical trial 28 days or 5 drug half-lives of the investigational agents prior to randomization * Received live vaccine 28 days prior to randomization * Treatment with unstable dosage of thrombopoietin receptor agonists such as Eltrombopag or Romiplostim 14 days prior to randomization * Subjects with depression or suicidal thoughts * Previous treatment with telitacicept * B cell targeting drug therapy is not tolerated or responsive * Investigator considers candidates not appropriating for the study

Primary outcome measure(s)

  • Overall response (CR + PR) rate — at week 24
    Response is deemed as complete (CR) if the platelet (PLT) count is ≥ 100×10\^9/L, partial (PR) if the platelet count ranges from 50×10\^9/L to 100×10\^9/L and at least doubled from baseline. No active bleeding is allowed in participants classified as CR or PR.

Trial sites (23)

FacilityCityRegionStatus
The First Affiliated Hospital of Anhui Medical College Hefei Anhui Recruiting
The First Affiliated Hospital of China University of Science and Technology (Anhui Provincial) Hefei Anhui Recruiting
Beijing Hospital Beijing Beijing Municipality Recruiting
Peking University People's Hospital Beijing Beijing Municipality Recruiting
Peking University Third Hospital Beijing Beijing Municipality Recruiting
First Affiliated Hospital, Sun Yat-Sen University Guangzhou Guangdong Recruiting
Guangdong Provincial People's Hospital Guangzhou Guangdong Recruiting
The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan Recruiting
Wuhan Union Hospital, China Wuhan Hubei Recruiting
Second Xiangya Hospital of Central South University Changsha Hunan Recruiting
Xiangya Hospital of Central South University Changsha Hunan Recruiting
The Affiliated Hospital of Inner Mongolia Medical University Hohhot Inner Mongolia Recruiting
First Hospital of China Medical University Shenyang Liaoning Recruiting
Shandong Provincial Hospital Jinan Shandong Recruiting
Changhai Hospital Shanghai Shanghai Municipality Recruiting
RenJi Hospital Shanghai Shanghai Municipality Recruiting
Shanxi Bethune Hospital Taiyuan Shanxi Recruiting
West China Hospital Chengdu Sichuan Recruiting
Institute of Hematology & Blood Diseases Hospital Tianjin Tianjin Municipality Recruiting
Tianjin First Central Hospital Tianjin Tianjin Municipality Recruiting
Tianjin Medical University General Hospital Tianjin Tianjin Municipality Recruiting
People's Hospital of Xinjiang Uygur Autonomous Region Ürümqi Xinjiang Uygur Autonomous Region Recruiting
The First People's Hospital of Yunnan Kunming Yunnan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05998759 on ClinicalTrials.gov ↗ ← All trials in China