Sirolimus Combined With Low-dose Warfarin for the Treatment of Refractory PNH

Phase 4

• Conditions: Paroxysmal Nocturnal Hemoglobinuria
• Interventions: Drug: sirolimus

• Registration Number: NCT03866681
• Lead Sponsor: Peking Union Medical College Hospital

Brief Summary

Classical paroxysmal nocturnal hemoglobinuria(PNH) is mainly characterized by hemolysis and thrombosis, which reduced patients ' quality of life(QoL) greatly and even lead to death. Glucocorticoids and symptomatic supportive therapy are traditional treatments and the response rate is far from satisfactory. Eculizumab is an effective therapy but it is expensive and not available in China mainland.The investigators aim to explore the efficacy and safety of sirolimus for refractory classic PNH.

Detailed Description

Classical paroxysmal nocturnal hemoglobinuria(PNH) is mainly characterized by hemolysis and thrombosis, which reduced patients ' quality of life(QoL) greatly and even lead to death. There is no ideal therapy except for eculizumab, expensive and not available in China mainland. Glucocorticoids and symptomatic supportive therapy are traditional treatments. The response rate is 30%, far from satisfactory. In recent years, T lymphocyte-mediated destruction of normal hematopoietic stem cells have been reported to involve the pathogenesis of PNH, making immunomodulatory drugs be potential effective treatments.

Sirolimus (rapamycin), produced by the bacterium Streptomyces hygroscopicus, is a mammalian target of Rapamycin (mTOR) inhibitor. mTOR is a serine/threonine kinase that regulates cell growth, proliferation, metabolism and survival. It has two interacting complex, mTORC1 and mTORC2. Sirolimus primarily inhibits mTORC1, has been demonstrated for its immunomodulatory effects and ability to improve hematopoietic stem cell function. Recently, sirolimus has been reported to be effective and well tolerated in the treatment of immune-mediated cytopenias, even in multi-immunosuppressants resistant patients. In addition, classical PNH patients have a higher risk of thrombosis especially in refractory ones and it is reasonable to use low-dose warfarin in the management of patients with classic refractory PNH.

In this study, it is anticipated to evaluate the effect of sirolimus combined with low-dose warfarin on patients with refractory classic PNH. The adverse effects and QoL on different time points were documented.

Study Timeline

• Study First Submitted: 2019-02-28
• Status Verified: 2019-03
• Study First Submitted QC: 2019-03-05
• Last Update Submitted: 2019-03-06
• Study First Posted: 2019-03-07
• Last Update Posted: 2019-03-08
• Study Start: 2019-04-01
• Primary Completion: 2021-03-01
• Study Completion: 2022-04-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• age 18-70 years
• diagnosed with PNH and no thrombosis
• ineffective, relapsed or intolerant to conventional treatment (eg glucocorticoids, • • iron, folic acid, androgen, etc.)
• not available for hematopoietic stem cell transplantation
• ECOG≤2
• agreed to sign the consent forms

Exclusion Criteria

• severe heart, liver and kidney dysfunction
• combined with thrombotic complications
• people who are pregnant and breastfeeding
• history of other immunosuppressive agents in recent 3 months
• Patients who are not eligible to participate in this trial due to any reason based • • • on the consideration of investigator

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Patients cohort	sirolimus	A total of 40 patients with refractory classic PNH will be included and will be intervened by a combined therapy including sirolimus and low-dose warfarin

Primary Outcome Measures

Name	Time	Method
Hemoglobin	2 years	Hemoglobin in g/L

Secondary Outcome Measures

Name	Time	Method
Short Form 36 items(SF-36) questionnaire	2 years	SF-36 questionnaire in scores

Trial Locations

Locations (1)

Peking union medical college hospital; 🇨🇳 Beijing, China