Background. Mesalazine enemas are of well proven efficacy t for the topical treatment of distal ulcerative colitis. Although new rectal formulations of mesalazine are not expected to be superior in efficacy and tolerability to standard formulations, they may offer secondary advantages in terms of overall acceptability. Aim. To compare the efficacy, tolerability and overall acceptability of a new mesalazine rectal foam (Salofalk'foam) with mesalazine enema in the treatment of active distal ulcerative colitis. ( Patients and Methods. A multicentre study was carried out in patients with active proctitis, proctosigmoiditis and left-sided ulcerative colitis as evaluated by the Clinical Activity Index (CAI 4) and Endoscopie Index (El 6). Patients were randomly assigned to receive, in open-label fashion, either f mesalazine foam 2 g nvice a day or mesalazine enema (2 g/60 ml t\vice a day) for 3 weeks. Patients who did not achieve remission (defined as CAI <4 and El <6) after 3 weeks contin-I lied the study receiving the alternative galenic formulation L for a further 3 weeks. f Results. A total of 195 patients were enrolled. Characteristics at baseline were similar except for concomitant therapy with oral 5-ASA products: during the 1st treatment phase, 47% of patients on enema received such treatment vs only 29% of those on foam. Patients with at least one post-treatment efficacy evaluation were included in the intent-to-treat analysis (n=89foam, n=-96 enema). After 3 weeks of treatment, 112 patients were in remission and only 59 patients entered the 2nd treatment phase thus providing data on acceptability. Remission was achieved after 3 weeks in 54% of patients treated with foam and in 67% of those treated with enema. The 90% confidence interval for the difference in remission rates was 0 to 24 and thus within the clinically acceptable range of therapeutic equivalence. At the end of the 2nd phase, 70% of patients switched to foam were in remission vs 65% to the enema. Two patients discontinued treatment with foam prematurely due to anal burning. No clinically important changes were seen in the laboratory tests. Conclusions. Salofaltf1 foam and enema are equally effective for the treatment ofproctitis, proctosigmoiditis and leftsided tilcerative colitis. 'The new foam preparation is as well tolerated and accepted as enemas and can be used as a therapeutic alternative to conventional mesalazine enema formulations.

Mesalazine foam (Salofalk® foam) in the treatment of active distal ulcerative colitis. a comparative trial vs Salofalk® enema / Ardizzone, S.; Doldo, P.; Ranzi, T.; Sturniolo, G. G.; Giglio, L. A.; Annese, V.; D'Arienzo, A.; Gaia, E.; Gullini, S.; Riegler, G.; Valentin, M.; Massa, P.; Del Piano, M.; Rossini, F.; Sategna Guidetti, C.; Fera, A.; Greinwald, R.; Bianchi Porro, G.. - In: ITALIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY. - ISSN 1125-8055. - 31:8(1999), pp. 669-674.

Mesalazine foam (Salofalk® foam) in the treatment of active distal ulcerative colitis. a comparative trial vs Salofalk® enema

Annese V.;
1999-01-01

Abstract

Background. Mesalazine enemas are of well proven efficacy t for the topical treatment of distal ulcerative colitis. Although new rectal formulations of mesalazine are not expected to be superior in efficacy and tolerability to standard formulations, they may offer secondary advantages in terms of overall acceptability. Aim. To compare the efficacy, tolerability and overall acceptability of a new mesalazine rectal foam (Salofalk'foam) with mesalazine enema in the treatment of active distal ulcerative colitis. ( Patients and Methods. A multicentre study was carried out in patients with active proctitis, proctosigmoiditis and left-sided ulcerative colitis as evaluated by the Clinical Activity Index (CAI 4) and Endoscopie Index (El 6). Patients were randomly assigned to receive, in open-label fashion, either f mesalazine foam 2 g nvice a day or mesalazine enema (2 g/60 ml t\vice a day) for 3 weeks. Patients who did not achieve remission (defined as CAI <4 and El <6) after 3 weeks contin-I lied the study receiving the alternative galenic formulation L for a further 3 weeks. f Results. A total of 195 patients were enrolled. Characteristics at baseline were similar except for concomitant therapy with oral 5-ASA products: during the 1st treatment phase, 47% of patients on enema received such treatment vs only 29% of those on foam. Patients with at least one post-treatment efficacy evaluation were included in the intent-to-treat analysis (n=89foam, n=-96 enema). After 3 weeks of treatment, 112 patients were in remission and only 59 patients entered the 2nd treatment phase thus providing data on acceptability. Remission was achieved after 3 weeks in 54% of patients treated with foam and in 67% of those treated with enema. The 90% confidence interval for the difference in remission rates was 0 to 24 and thus within the clinically acceptable range of therapeutic equivalence. At the end of the 2nd phase, 70% of patients switched to foam were in remission vs 65% to the enema. Two patients discontinued treatment with foam prematurely due to anal burning. No clinically important changes were seen in the laboratory tests. Conclusions. Salofaltf1 foam and enema are equally effective for the treatment ofproctitis, proctosigmoiditis and leftsided tilcerative colitis. 'The new foam preparation is as well tolerated and accepted as enemas and can be used as a therapeutic alternative to conventional mesalazine enema formulations.
1999
Mesalazine
Rectal foam
Topical treatment
Ulcerative colitis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/172653
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