MedPath

A Double-blind, Double-dummy, Parallel, Active-controlled, Randomized Trial to Evaluate Efficacy & Safety in Anemia Subjects

Phase 3
Completed
Conditions
Iron Deficiency Anemia
Interventions
Drug: Polyferose
Other: Placebo to Polyferose
Other: Placebo to Ferrous (II) Glycine Sulphate Complex
Registration Number
NCT01425463
Lead Sponsor
Sanol GmbH
Brief Summary

To evaluate the efficacy and safety of 12 weeks treatment with Ferrous (II) Glycine Sulphate Complex in comparison to Polyferose capsules in Chinese subjects with manifest Iron Deficiency Anemia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
256
Inclusion Criteria
  • An iron deficiency anemia patient with Serum Ferritin < 12 ng/mL, serum Hb-values >60 and < 120 g/L in males, < 110 g/L in females
Exclusion Criteria
  • With any Mal-absorption Syndrome
  • With a history of Thalassemia or Sickle Cell Anemia
  • With untreated concurrent Vitamin B12 or Folate deficiency at Baseline

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ferrous (II) Glycine Sulphate ComplexFerrous (II) Glycine Sulphate ComplexFerrous (II) Glycine Sulphate Complex treatment with 567.7 mg three times a day (t.i.d.) for 12 weeks plus Placebo to Polyferose.
Ferrous (II) Glycine Sulphate ComplexPlacebo to PolyferoseFerrous (II) Glycine Sulphate Complex treatment with 567.7 mg three times a day (t.i.d.) for 12 weeks plus Placebo to Polyferose.
PolyferosePlacebo to Ferrous (II) Glycine Sulphate ComplexPolyferose treatment with 150 mg twice daily (b.i.d) for 12 weeks plus Placebo to Ferrous (II) Glycine Sulphate Complex.
PolyferosePolyferosePolyferose treatment with 150 mg twice daily (b.i.d) for 12 weeks plus Placebo to Ferrous (II) Glycine Sulphate Complex.
Primary Outcome Measures
NameTimeMethod
Change in Hemoglobin (Hb) From Baseline (Week 0) to Week 12From Baseline to Week 12
Secondary Outcome Measures
NameTimeMethod
Change in Hemoglobin (Hb) From Baseline (Week 0) to Week 2From Baseline to Week 2
Change in Hemoglobin (Hb) From Baseline (Week 0) to Week 4From Baseline to Week 4
Change in Hemoglobin (Hb) From Baseline (Week 0) to Week 8From Baseline to Week 8
Percentage of Responders at Week 12End of Treatment Period (Week 12)

Responders are defined as having an increment of Hemoglobin (Hb) \> 15 g/L and post-treatment Hb \> 120 g/L (male) or \> 110 g/L (female) at Visit 6 (Week 12).

Trial Locations

Locations (15)

5

🇨🇳

Hangzhou, China

6

🇨🇳

Hangzhou, China

10

🇨🇳

Guangzhou, China

7

🇨🇳

Jinan, China

14

🇨🇳

Shanxi, China

17

🇨🇳

Wenzhou, China

4

🇨🇳

Wuxi, China

9

🇨🇳

Xi'an, China

13

🇨🇳

Shanxi, China

1

🇨🇳

Fuzhou, China

15

🇨🇳

Changsha, China

16

🇨🇳

Changsha, China

8

🇨🇳

Jinan, China

12

🇨🇳

Shenyang, China

2

🇨🇳

Tianjin, China

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