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Kusajili – Clinical trials directory
Result
of your search per sponsor: Pharmacosmos A/S
Woman Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
Treatment of pregnant women with iron deficiency anemia
The primary objective of the trial is to evaluate and compare the effect of IV iron isomalto-side to a fixed dose of oral iron administered as tablet ferrous fumarate with ascorbic acid as correction ...
Country
None
organs
None
Specialty
None
unknown
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Woman Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
Treatment of women after severe Postpartum Haemorrhage
The primary objective of this study is to get explorative information about IV high single dose infusion of iron isomaltoside 1000 compared to RBC transfusion in the treatment of severe PP-IDA evaluat...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A study of intravenous iron isomaltoside 1000 (Monofer®) compared to placebo in subjects with iron deficiency anaemia who are Intolerant or unresponsive to oral iron therapy
The primary objective of the study is to evaluate and compare the effect of iron isomaltoside 1000 to placebo in its ability to increase haemoglobin (Hb) in subjects with IDA when oral iron preparatio...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A phase III, randomized, comparative, open-label study of intravenous iron oligosaccharide (Monofer®) administered by infusions or repeated bolus injections in comparison with oral iron sulphate in inflammatory bowel disease subjects with iron deficiency anaemia
To demonstrate that intravenous iron oligosaccharides is non-inferior to oral iron sulphate in reducing iron deficiency anaemia secondary to IBD, evaluated as the ability to increase haemoglobin (Hb).
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A Randomized, Prospective, Double-Blind, Comparative Placebo-Controlled Study of Intravenous Iron Isomaltoside 1000 (Monofer®) administered by Infusions to Iron-Deficient Blood Donors
The primary efficacy objective of the study is to evaluate the effect of IV iron isomaltoside 1000 compared with placebo in first-time female donors with p-ferritin below 60 µg/L. The safety objecti...
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
Treatment of Women after Postpartum Haemorrhage
The primary objective of this study is to compare efficacy of IV high single dose infusion of iron isomaltoside 1000 to standard medical care in women with PPH evaluated as physical fatigue.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A non-comparative open-label study of Iron Oligosaccharide in CHF patients with iron deficiency (either absolute or functional) anaemia and a need for parenteral iron
The primary objective of the present study is to obtain safety reassurance with the use of Iron oligosaccharide given either as repeated IV boluses or as total dose infusion (TDI) for the correction o...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A clinical Safety Study of the medicinal product Monofer given into a vein and administered by a High Dosing Regimen in patients with Inflammatory Bowel Disease
The primary objective of the study is to evaluate the safety of a high IV iron dosing regimen of iron iso-maltoside 1000 in subjects with IDA secondary to IBD.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
This long-term follow-up study will assess the ability to maintain a stable haemoglobin (iron containing molecule in the blood) and safety profile of iron isomaltoside 1000 (Monofer®) in Inflammatory Bowel Disease subjects with iron deficiency anemia
1. To assess the long term efficacy of iron isomaltoside 1000 (Monofer®) by means of the ability to maintain stable Hb (defined as Hb ≥ 12.0 g/dL) in subjects with Hb ≥ 12.0 g/dL at the Baseline of Ex...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pharmacosmos A/S
Update Il y a 4 ans
A non-comparative open-label study of Iron Oligosaccharide in Chronic Kidney Disease patients with a need for parenteral iron
The primary objective of the present study is to obtain such safety reassurance with the use of Iron Oligosaccharide given either as repeated IV boluses or as total dose infusion (TDI) for correction/...
Country
None
organs
None
Specialty
None
Closed trial
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