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Completed

NCT Number: NCT04146207

SHR0302 and Steroid As First Line Therapy for Chronic GVHD

The purpose of this study is to evaluate the efficacy of SHR0302 in combination with Prednisone as first line therapy in patients with moderate to severe chronic graft-versus-host disease (GVHD).

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Shanghai General Hospital, Shanghai, Shanghai Municipality, China

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About this study

Treatment: Once patients are diagnosed with chronic GVHD, the combination therapy should be initiated as soon as possible. 1. Prednisone: 1mg/kg/d po. Taper steroid every two weeks according to patient's response. 2. SHR0302 QD po. for at least 28 days. Indication for stopping SHR0302 treatment: 1. No response after SHR0302 treatment for 12 weeks. 2. Develop life-threatening complication. 3. ANC<0.5×10e9/L or PLT< 30×10e9/L.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥ 18 years old and ≤ 70 years old, male or female;
  • Patients receiving allogeneic peripheral blood stem cell transplantation for hematological diseases;
  • The primary hematological malignancies are completely relieved and are expected to be stable for at least 3 months;
  • Chronic GVHD that was first attacked after transplantation and at least 100 days after transplantation, reached a moderate or severe level by NIH classification;
  • There was no previous systemic treatment (including in vitro illumination [ECP]);
  • The patient may be receiving other immunosuppressive agents to prevent or treat acute GVHD, but if the subject receives prednisone to prevent or treat acute GVHD, it must be <0.5 mg/kg/d or equivalent dose of other glucocorticoids;
  • The chronic GVHD that has started hormone therapy does not exceed 72 hours;
  • Karnofsky score > 60 points;
  • Patients must be able to understand and are willing to participate in the study and sign an informed consent form.

Exclusion criteria

  • Can not tolerate prednisone dose 1mg / kg / d or equivalent dose of other glucocorticoids for the treatment of cGVHD;
  • Receive any systemic treatment of cGVHD, except for corticosteroids that treat cGVHD within 72 hours prior to the signing of informed consent;
  • Patients with GVHD overlap syndrome (NIH criteria);
  • Treatment of acute GVHD has received other Jak inhibitors such as ruxolitinib;
  • Pregnant or lactating women;
  • The patient is judged by the investigator to have complications that may cause other risks;
  • The patient is receiving other study medications;
  • Patient blood routine: ANC <1.0 × 109 / L or PLT < 50 × 109 / L;
  • Non-GVHD-related liver damage: the aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ratio is more than 3 times normal or the direct bilirubin normal value is more than 3 times;
  • Renal dysfunction: endogenous creatinine clearance (Ccr) < 50mL/min or normal serum creatinine 1.5 times or more, regardless of hemodialysis treatment;
  • Uncontrolled infections: hemodynamic instability associated with infection, or new signs or signs of infection, or new infections in imaging, persistent fever without symptoms or signs and cannot be ruled out Infected person
  • People living with HIV;
  • Active hepatitis B (HBV), active hepatitis C (HCV) requires antiviral therapy; patients with HBV activation risk refer to patients with hepatitis B surface antigen-positive or core antibody-positive patients who are not treated with anti-HBV;
  • The patient's primary malignant disease recurs and the graft is rejected;
  • Those who are allergic to known JAK inhibitors.

Treatment and study plan

SHR0302

Drug

SHR0302 po QD

Prednisone

Drug

Prednisone 1mg/kg/d po

Primary outcomes

  1. Safety and tolerability of SHR0302 and prednisone

    Time frame: After the first dose of SHR0302 or prednisone until 30 days after the last dose of SHR0302 or prednisone.

    The severity of adverse events is determined according to the CTCAE V5.0 criteria.

Secondary outcomes

  1. Overall response rate (ORR) at week 4

    Time frame: Within 4 weeks

    Response rate at week 4 (the proportion of responders [CR or PR]) as defined by the NIH Consensus Development Project (2014)

  2. Overall response rate (ORR) at week 24

    Time frame: Within 24 weeks

    Response rate at week 24 (the proportion of responders [CR or PR]) as defined by the NIH Consensus Development Project (2014)

Sponsors and collaborators

Lead sponsor

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study title

SHR0302 and Prednisone As First Line Therapy for Chronic Graft Versus Host Disease Following Allogeneic Stem Cell Transplantation

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Oct 31, 2019
Registry last updated
Nov 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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