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Kusajili – Clinical trials directory
Result
of your search per sponsor: Institut de Recherches Internationales Servier (I.R.I.S)
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
Follow-up trial with no study drug prescription in diabetic patients previously included in the REGULATE trial
To document the clinical condition of patients who were included in the REGULATE trial and exposed to the investigational drugs (benfluorex or pioglitazone).
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
Assessment of the acceptability of a sublingual formulation of piribedil (S90049), 10 to 30 mg on request (maximum 5 times a day) on the top of L-dopa and a dopamine agonist in advanced Parkinson Disease patients with motor fluctuations: a 4-week open label pilot study
Assessment of the acceptability of a sublingual formulation of piribedil
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
A study to evaluate the long-term safety of patients with advanced lymphoid malignancies who have been previously administered with UCART19
To evaluate the long-term safety of patients with advanced lymphoid malignancies who have been previously administered with UCART19.
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
Evaluation of administration of gevokizumab versus placebo on the reduction of atheroma plaque inflammation
The primary objective is to evaluate the effect of gevokizumab on arterial wall inflammation reduction following a recent Acute Coronary Syndrome (ACS)
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
A study to evaluate the safety and tolerability of ascending doses of UCART19 given as a single infusion in patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukaemia (ALL) and to determine the maximum tolerated dose (MTD)
To evaluate the safety and tolerability of several doses of UCART19 in patient with relapsed/refractory (R/R) acute lymphoblastic leukaemia (ALL) and to determine the maximum tolerated dose (MTD).
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Institut de Recherches Internationales Servier (I.R.I.S)
Update Il y a 4 ans
Long-term (3 years) ophthalmic safety and cardiac efficacy and safety of ivabradine administered orally at the therapeutic doses (2.5/5/7.5 mg b.i.d.) on top of anti-anginal background therapy, to patients with chronic stable angina pectoris. An international, double-blind placebo controlled study
- To document the absence of retinal toxicity of ivabradine versus placebo in chronic stable angina patients after treatment cessation in the subset of patients with emergent bilateral relevant ERG ab...
Country
None
organs
None
Specialty
None
unknown
More information