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A Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors

Primary Purpose

Hematological Malignancy, Cancer-Related Anemia

Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Shengxuening Tablet
Ferrous succinate
Sponsored by
Zhongnan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hematological Malignancy focused on measuring Shengxuening tablet, chemotherapy-related Anemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age>18 years old, gender is not limited; Patients diagnosed with blood cancer complicated with anemia; During the screening period of ≤1 week, hemoglobin (Hb): 60g/L<Hb≤100g/L; Willingness to treat Exclusion Criteria: During the screening period of ≤1 week, hemoglobin (Hb)≤60g/L History of blood transfusion within 1 month; Urgent blood transfusion or EPO infusion is required within the screening period of ≤1 week; Folic acid or vitamin B12 deficiency; History of iron allergy, history of allergy or intolerance to the study drug; Pregnant and lactating women; Age <18 years old and body weight ≤35kg; Participated in other clinical drug research in the past 3 months; Severe cardiac insufficiency (NYHA grade III or above); Severe abnormal liver function (ALT, AST and TBIL ≥ 2 times the upper limit of normal value); Severe renal insufficiency (creatinine clearance ≤ 15ml/min); Severe mental disorder; Acute and chronic blood loss; Combined with a second tumor; Ferritin>500μg/L; Combined with active tuberculosis; Failure to cooperate with treatment according to doctor's advice.

Sites / Locations

  • Zhongnan Hospital of Wuhan UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Shengxuening Tablets

ferrous succinate

Arm Description

Oral treatment with Shengxuening Tablets 1 week before chemotherapy, usage: 0.5gtid, for 28 consecutive days

Oral treatment with ferrous succinate 1 week before chemotherapy, usage: 200mgqd, for 28 consecutive days

Outcomes

Primary Outcome Measures

Change from Blood routine in plasma at Week 4
Hemoglobin in g/L
Change from Blood routine in plasma at Week 4
Red Blood Cell in 10^12/L
Change from Blood routine in plasma at Week 4
mean corpuscular hemoglobin in pg
Change from Blood routine in plasma at Week 4
mean corpuscular volume in fL
Change from Blood routine in plasma at Week 4
Red blood cell specific volume in percentage
Change from Blood routine in plasma at Week 4
Reticulocyte in 10^9/L
Change from Blood routine in plasma at Week 4
Serum erythropoietin in ng/ml

Secondary Outcome Measures

Changes from iron metabolism indicators in plasma at week 4
serum ferritin in μg/L
Changes from iron metabolism indicators in plasma at week 4
serum iron in μmol/L
Changes from iron metabolism indicators in plasma at week 4
total iron binding capacity in μmol/L
Changes from iron metabolism indicators in plasma at week 4
unsaturated iron binding capacity in μmol/L
Changes from iron metabolism indicators in plasma at week 4
transferrin saturation in percentage

Full Information

First Posted
February 25, 2023
Last Updated
August 23, 2023
Sponsor
Zhongnan Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05784870
Brief Title
A Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors
Official Title
A Multicenter Randomized Controlled Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 7, 2023 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhongnan Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Cancer-related anemia (CRA) is one of the common accompanying diseases of malignant tumors. In 2019, a cross-sectional survey on the anemia status of 7324 malignant tumor patients in 97 hospitals in China found that the incidence of CRA was about 49.24%. 92.84% of the patients have not been given enough attention and effective treatment. According to the European Oncological Anemia Survey, CRA has the highest incidence in leukemia patients, followed by lymphoma/myeloma. CRA not only leads to a decline in the quality of life of patients, but also reduces the sensitivity to radiotherapy and chemotherapy, and also causes hypoxia in tumor tissue, which affects the prognosis of patients as an independent factor. At present, the treatment of CRA mainly includes blood transfusion therapy, erythropoiesis-stimulating agent (ESA) therapy, iron supplementation, etc. Conventional oral iron has low bioavailability and strong gastrointestinal irritation. Although intravenous iron can quickly replenish iron, excessive iron supplementation is prone to iron overload. Less acceptable. Shengxuening Tablets are derived from silkworm excrement. The main components of iron chlorophyllin and chlorophyll derivatives are very similar in structure to heme, and can be directly absorbed by small intestinal mucosal cells, effectively supplementing the iron elements required in the process of hematopoiesis. The investigators found that Shengxuening Tablets can increase the number of peripheral blood cells in mouse models of myelosuppression, improve bone marrow morphology, reverse the decrease in body weight and spleen index, and increase the levels of serum erythropoietin and granulocyte-macrophage colony-stimulating factor . Real-time fluorescent quantitative PCR and Western blot analysis showed increased expression levels of stem cell factor (SCF), JAK2 and STAT3 in the liver. These results indicated that Shengxuening Tablets promoted the recovery of hematopoietic function in myelosuppressive models by increasing the secretion of hematopoietic factors and activating the JAK2/STAT3 pathway. Therefore, in order to further confirm the preventive effect, effectiveness and safety of Shengxuening Tablets in the treatment of anemia in patients with hematological tumors complicated with anemia, this clinical trial was designed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hematological Malignancy, Cancer-Related Anemia
Keywords
Shengxuening tablet, chemotherapy-related Anemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
168 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Shengxuening Tablets
Arm Type
Experimental
Arm Description
Oral treatment with Shengxuening Tablets 1 week before chemotherapy, usage: 0.5gtid, for 28 consecutive days
Arm Title
ferrous succinate
Arm Type
Active Comparator
Arm Description
Oral treatment with ferrous succinate 1 week before chemotherapy, usage: 200mgqd, for 28 consecutive days
Intervention Type
Drug
Intervention Name(s)
Shengxuening Tablet
Intervention Description
Oral treatment with Shengxuening Tablets 1 week before chemotherapy, usage: 0.5gtid, for 28 consecutive days
Intervention Type
Drug
Intervention Name(s)
Ferrous succinate
Intervention Description
Oral treatment with ferrous succinate 1 week before chemotherapy, usage: 200mgqd, for 28 consecutive days
Primary Outcome Measure Information:
Title
Change from Blood routine in plasma at Week 4
Description
Hemoglobin in g/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
Red Blood Cell in 10^12/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
mean corpuscular hemoglobin in pg
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
mean corpuscular volume in fL
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
Red blood cell specific volume in percentage
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
Reticulocyte in 10^9/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Change from Blood routine in plasma at Week 4
Description
Serum erythropoietin in ng/ml
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Secondary Outcome Measure Information:
Title
Changes from iron metabolism indicators in plasma at week 4
Description
serum ferritin in μg/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Changes from iron metabolism indicators in plasma at week 4
Description
serum iron in μmol/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Changes from iron metabolism indicators in plasma at week 4
Description
total iron binding capacity in μmol/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Changes from iron metabolism indicators in plasma at week 4
Description
unsaturated iron binding capacity in μmol/L
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4
Title
Changes from iron metabolism indicators in plasma at week 4
Description
transferrin saturation in percentage
Time Frame
Day 0,Week 1,Week2,Week 3,Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age>18 years old, gender is not limited; Patients diagnosed with blood cancer complicated with anemia; During the screening period of ≤1 week, hemoglobin (Hb): 60g/L<Hb≤100g/L; Willingness to treat Exclusion Criteria: During the screening period of ≤1 week, hemoglobin (Hb)≤60g/L History of blood transfusion within 1 month; Urgent blood transfusion or EPO infusion is required within the screening period of ≤1 week; Folic acid or vitamin B12 deficiency; History of iron allergy, history of allergy or intolerance to the study drug; Pregnant and lactating women; Age <18 years old and body weight ≤35kg; Participated in other clinical drug research in the past 3 months; Severe cardiac insufficiency (NYHA grade III or above); Severe abnormal liver function (ALT, AST and TBIL ≥ 2 times the upper limit of normal value); Severe renal insufficiency (creatinine clearance ≤ 15ml/min); Severe mental disorder; Acute and chronic blood loss; Combined with a second tumor; Ferritin>500μg/L; Combined with active tuberculosis; Failure to cooperate with treatment according to doctor's advice.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhou Fuling
Phone
18986265580
Email
zhoufuling@163.com.cn
Facility Information:
Facility Name
Zhongnan Hospital of Wuhan University
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430071
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhou Fuling, director
Phone
+86-02767813137
Email
zhoufuling@163.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

A Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors

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