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dc.contributor.authorSezer, Zafer
dc.contributor.authorInal, Ahmet
dc.contributor.authorCinar, Salih L.
dc.contributor.authorMazicioglu, Mustafa M.
dc.contributor.authorAltug, Sedat
dc.contributor.authorKarasulu, Hatice Y.
dc.contributor.authorDiril, Mine
dc.date.accessioned2024-02-04T13:29:39Z
dc.date.available2024-02-04T13:29:39Z
dc.date.issued2023
dc.identifier.issn2193-8210
dc.identifier.issn2190-9172
dc.identifier.urihttps://doi.org/10.1007/s13555-023-00939-7
dc.identifier.urihttp://hdl.handle.net/11446/4709
dc.description.abstractIntroductionPsoriasis is a common skin disorder associated with physical and psychological burdens. Visible disfiguration can trigger a negative reaction which can cause much of the readily measurable psychological burden of the disease. Although many biological treatments provide some success in the initial clearance of lesions, there is a dispute about the long-term maintenance of the disease, as no current biological treatment has been shown to be curative. Topical therapies are still the most widely used agents as first-line and maintenance treatment for psoriasis. The present study aimed to investigate the safety, tolerability, and, to some extent, efficacy of GN-037 cream in patients with psoriasis and healthy volunteers.MethodsA randomized, double-blind, single-center, placebo-controlled phase 1 clinical study was conducted to evaluate the safety, tolerability, and clinical efficacy of GN-037 cream topically applied twice daily for 2 weeks in healthy subjects (n = 12) and patients (n = 6) diagnosed with plaque-type psoriasis. Six healthy subjects received placebo. Patients with plaque psoriasis were evaluated by a dermatologist, and Physician Global Assessment (PGA) score was required to be >= 3 (moderate psoriasis) at screening.ResultsA total of 31 adverse events (AEs) occurred in 13 participants during the study: 9 AEs in healthy subjects receiving GN-037 cream, 3 AEs in healthy subjects receiving placebo, and 1 AE in one psoriatic patient. The most frequently reported AEs were reactions at the application site, including erythema, exfoliation, pruritus, and burning sensation. During the baseline evaluation, one patient had a PGA score of 3 (moderate) and five patients had a PGA score of 4 (severe). On day 14, in treatment, four patients experienced second grade and two patients third grade improvements compared with baseline, indicating a shift of patients from moderate and severe disease to mild disease and to almost clear (score 2 or 1). There were slight increases in plasma tumor necrosis factor (TNF)-alpha, interleukin-17 (IL-17) and interleukin-23 (IL-23) levels in both healthy volunteers and patients throughout the study, as compared with baseline.ConclusionThe results of this phase 1 trial conducted in 18 healthy volunteers and 6 patients with plaque psoriasis demonstrated a favorable safety and tolerability profile for GN-037; therefore, further clinical development of GN-037 in a phase 2 clinical trial has been initiated in patients with mild to moderate plaque psoriasis (NCT05706870).en_US
dc.description.sponsorshipGen Ilalve Saglik Urunleri A.S.; Scientific and Technological Research Council of Turkey [TUBITAK 1505, 5180004]en_US
dc.description.sponsorshipThis study was sponsored by Gen Ilalve Saglik Urunleri A.S. and partially supported by a research grant from The Scientific and Technological Research Council of Turkey [TUBITAK 1505, grant number: 5180004]. The journal's Rapid Service Fee is funded by Gen Ilalve Saglik Urunleri A.S.en_US
dc.language.isoengen_US
dc.publisherAdis Int Ltden_US
dc.relation.ispartofDermatology And Therapyen_US
dc.identifier.doi10.1007/s13555-023-00939-7
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGN-037en_US
dc.subjectPhase 1en_US
dc.subjectPlaque psoriasisen_US
dc.subjectTopical treatmenten_US
dc.titleSafety and Efficacy of a Novel Combination Cream (GN-037) in Healthy Volunteers and Patients with Plaque Psoriasis: A Phase 1 Trialen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue7en_US
dc.identifier.volume13en_US
dc.identifier.startpage1489en_US
dc.identifier.endpage1501en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Sezer, Zafer; Inal, Ahmet] Erciyes Univ, Fac Med, Dept Pharmacol, Kayseri, Turkiye; [Sezer, Zafer; Inal, Ahmet] Erciyes Univ, Hakan Cetinsaya Good Clin Practice & Res Ctr IKUM, Kayseri, Turkiye; [Cinar, Salih L.] Erciyes Univ, Fac Med, Dept Dermatol, Kayseri, Turkiye; [Mazicioglu, Mustafa M.] Erciyes Univ, Fac Med, Dept Family Med, Kayseri, Turkiye; [Altug, Sedat] Demiroglu Bilim Univ, Fac Med, Dept Pharmacol, Istanbul, Turkiye; [Karasulu, Hatice Y.] Ege Univ, Fac Pharm, Dept Pharmaceut Technol, Izmir, Turkiye; [Karasulu, Hatice Y.] Ege Univ, Ctr Drug R&D & Pharmacokinet Applicat Argefar, Izmir, Turkiye; [Diril, Mine; Mehmetoglu, Al Ayca] Sedef Ilac & Med Urunleri Ind Trade Co Ltd, Dept Res & Dev, Kastamonu, Turkiye; [Kozlu, Serhat; Ulu, Nadir] Gen Ilac & Saglik Urunleri AS, Dept Res & Dev, ASO 2 & 3 Organize Sanayi Bolgesi, Alci OSB Mahall, TR-06930 Ankara, Turkiyeen_US
dc.authoridkarasulu, Hatice Yesim/0000-0002-1860-8255
dc.authoridUlu, Nadir/0000-0002-2681-8615
dc.identifier.pmid37300792en_US
dc.identifier.scopus2-s2.0-85161397930en_US
dc.identifier.wosWOS:001004065400002en_US
dc.authorwosidkarasulu, Hatice Yesim/HPG-4201-2023


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