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March 11, 2013
Sanofi and Regeneron Pharmaceuticals issued pooled results from two phase Ib trials of dupilumab for atopic dermatitis. The trials enrolled a total of 67 subjects with moderate-to-severe atopic dermatitis not adequately controlled with topical medications. The subjects were randomized to three different doses of dupilumab (75mg, 150mg or 300mg) or placebo administered as weekly subcutaneous injections for four weeks. The efficacy data showed treatment with dupilumab at either 150mg or 300mg per week significantly improved the signs and symptoms of atopic dermatitis, with significant improvements in body surface area (BSA) score, Investigator Global Assessment (IGA) score and Eczema Area Severity Index (EASI) from baseline to week four, compared to placebo (p<0.05 vs. placebo for all measures and doses). The significant improvements in BSA, IGA and EASI scores were maintained at week eight in the 300mg dose group (p<0.05 vs. placebo). The most common adverse events were nasopharyngitis and headaches. A phase IIa trial is currently underway and a phase IIb trial is planned for later this year.
December 19, 2011
Anacor released results from two phase IIa trials of AN2728 and AN2898 for the treatment of atopic dermatitis. The six-week, double-blind, randomized trials enrolled 46 subjects with mild to moderate atopic dermatitis. Skin lesions were treated with 2% AN2728, 1% AN2898 or placebo ointments twice daily. The primary outcome measure was improvement of lesions for each treatment group, measured by the Atopic Dermatitis Severity Index (ADSI) score at 28 days post-treatment. The primary endpoint for both compounds was successfully achieved after 28 days of twice-daily treatment, with 64% of AN2728-treated lesions showing improvement on the ADSI score versus 24% for placebo (p≡0.05) and 71% of AN2898-treated lesions showing improvement on the ADSI score versus 14% for placebo (p≡0.01).
December 20, 2010
Creabilis issued positive results from a phase IIa trial of CT327 for the treatment of atopic dermatitis. This trial enrolled 15 subjects in Switzerland who received CT327 topically 0.1% cream twice daily for 15 days or placebo. A clinically significant improvement in symptoms was seen after eight days of treatment with CT327, as measured by change in mEASI (modified eczema area and severity index) score from baseline. Onset of efficacy was seen at three to five days of treatment. The greatest patient-reported benefit was in nighttime itch. CT327 was safe and well tolerated with no serious adverse events and no reported site irritation.
February 25, 2008
JADO Technologies issued positive results from a phase II trial of TF002 for the treatment of atopic dermatitis. This randomized, double-blind, active controlled trial enrolled seventeen subjects who received TF002 or hydrocortisone. The primary endpoint was the reduction of inflammation in atopic skin after three weeks, measured through a highly significant improvement in TIS (Three Item Severity) score. The endpoint was reached; both TF-002 and hydrocortisone improved three item severity scores by more than 1.5. At a four week follow-up, TF-002 showed continued benefit and did not induce skin atrophy when compared with hydrocortisone. TF002 also showed a trend towards reducing the total number of mast cells. Based on the results, JADO plans to move forward with the development of TF002.
July 9, 2007
Cytos issued mixed results from a phase IIa trial of CYT-003-QbG10 for the treatment of atopic dermatitis (AD). This randomized, double-blind and placebo-controlled trial enrolled 36 subjects withmild to moderate AD, as assessed by the Eczema Area Severity Index (EASI). Subjectswere randomized to two treatment groups and received 6 weekly subcutaneous injectionsof either 300 micrograms CYT003-QbG10 or placebo. Two weeks after the last dose,the disease status of the patients was again assessed by the EASI. Treatment wassafe and well tolerated. However, both the CYT003-QbG10 and placebo treatmentgroups showed a similar reduction of the EASI scores as measured over the studyperiod, indicating no treatment effect for CYT003-QbG10 in atopic dermatitis atthe dose level tested in this trial. Based on the results, Cytos is planning toconduct trials testing higher dose levels of CYT-003-QbG10 in order to determinea future path for this compound.