Dr. Wolf-Achim Hassenpflug

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Universitaetsklinikum Hamburg-Eppendorf

Studies Thrombotic Thrombocytopenic Purpura
Studies TTP
3 reported clinical trials
5 drugs studied

Area of expertise

1Thrombotic Thrombocytopenic Purpura
Wolf-Achim Hassenpflug has run 2 trials for Thrombotic Thrombocytopenic Purpura. Some of their research focus areas include:
ADAMTS13 positive
ADAMTS-13 positive
ADAMTS-13 negative
2TTP
Wolf-Achim Hassenpflug has run 2 trials for TTP. Some of their research focus areas include:
ADAMTS13 positive
ADAMTS-13 positive
ADAMTS-13 negative

Clinical Trials Wolf-Achim Hassenpflug is currently running

Image of trial facility.

TAK-755

for Purpura

Thrombotic thrombocytopenic purpura (or TTP for short) is a condition where blood clots form in small blood vessels throughout the body. The clots can limit or block the flow of oxygen-rich blood to the body's organs, such as the brain, kidneys, and heart. As a result, serious health problems can develop. The increased clotting that occurs in TTP uses up the cells that help the blood to clot, called platelets. With fewer platelets available in the blood, bleeding problems can also occur. People who have TTP may bleed underneath the skin forming purple bruises, or purpura. TTP also can cause anemia, a condition in which red blood cells break apart faster than the body can replace them, leading to fewer red blood cells than in normal. TTP is caused by a lack of activity in the ADAMTS13 enzyme, a protein in the blood involved in controlling clotting of the blood. The ADAMTS13 enzyme breaks up another blood protein called von Willebrand factor that forms blood clots by clumping together with platelets. Some people are born with this condition, while others develop the condition during their life. Many people who are born with TTP experience frequent flare-ups that need to be treated right away. TAK-755 is a medicine that replaces ADAMTS13 and may prevent or control TTP flare-ups, called acute TTP events. The main aim of the study is to check for side effects of long-term treatment with TAK-755. Treatment will be given in 2 ways: 1. TAK-755 treatment given either every week or every other week to prevent acute TTP events from happening (the "prophylactic" cohort). 2. TAK-755 treatment given to control an acute TTP event when it happens (the "on-demand" cohort). Participants in the prophylactic cohort will receive treatment in the clinic or at home for up to approximately 3 years. They will visit the clinic at least every 12 weeks. Participants in the on-demand cohort will receive daily treatment for the acute TTP event until the flare-up has gotten better. They will have a follow-up visit at the clinic 4 weeks later.
Recruiting2 awards Phase 310 criteria
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rVWF +/− ADVATE

for Von Willebrand Disease

The main aim of the study is to check effectiveness, side effects, and tolerability of vonicog alfa (recombinant von Willebrand factor \[rVWF\]), with or without ADVATE, in the treatment and control of nonsurgical bleeding events in pediatric participants (less than (\<)18 years of age) with severe hereditary von Willebrand disease (VWD). The participants will be treated with vonicog alfa for 12-18 months. Their von Willebrand Disease will be treated by their doctor according to their doctor's usual clinical practice. During the study, participants will be followed up at clinics or over telephone calls.
Recruiting2 awards Phase 3

More about Wolf-Achim Hassenpflug

Clinical Trial Related4 years of experience running clinical trials · Led 3 trials as a Principal Investigator · 2 Active Clinical Trials
Treatments Wolf-Achim Hassenpflug has experience with
  • Antihemophilic Factor (Recombinant)
  • Von Willebrand Factor (Recombinant)
  • BAX 930
  • Standard Of Care
  • TAK-755
Breakdown of trials Wolf-Achim Hassenpflug has run
Thrombotic Thrombocytopenic Purpura

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