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Next Level Education Acquires Summit Mortgage Training

Next Level Education Acquires Summit Mortgage Training

Business Wire15-05-2025

FRANKLIN, Tenn.--(BUSINESS WIRE)-- Next Level Education (NLE), a provider of continuing education and training for the mortgage industry, announces it has acquired Summit Mortgage Training of Hanover, NJ. Andrea Gagliardi, founder of Summit, has joined the Next Level team as Director of Content Management.
'This acquisition was a strategic decision on our part to accelerate the growth of Next Level Education while expanding our access to mortgage professionals along the East Coast, empowering them with cutting-edge education options and industry-leading expertise,' said J.R. Huber, Co-Founder and CEO/President of NLE.
Debbie Gadberry, Co-Founder and COO/Senior Vice President of NLE, added, 'By acquiring Summit, we have immediately grown our content offerings to provide an even more robust and comprehensive training suite for the mortgage industry.'
Summit Mortgage Training was founded eight years ago by Gagliardi, who delivered pre-licensing education and NMLS Continuing Education (CE) courses as well as other training offerings throughout New Jersey, Pennsylvania, and Florida. Among the new courses that will be offered by NLE are 'Ninety Days to Impact!,' a 13-week coaching program for new loan officers designed to increase organizations and referral sources, and 'Mortgage Fundamentals,' an introductory course on the mechanics of loan originations.
To learn more about NLE and its innovative approach to professional development, go to https://nextleveled.com/.
About Next Level Education
An NMLS-approved provider, Next Level Education is redefining mortgage education and professional development. Leveraging modern tools like Adobe Learning Manager, it delivers impactful training and continuous education programs while keeping professionals informed with the latest industry news and updates. Its mission is to empower aspiring and experienced mortgage professionals with licensing and education courses that are accessible, interactive, and fun. For more information, call 615.899.5343 or visit www.nextleveled.com.

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Denifanstat has the potential to be a first-in-class, once-daily, oral acne therapeutic, potentially offering both exceptional efficacy and patient compliance with a favorable safety and tolerability profile. Compared to other oral acne treatments, denifanstat provides outstanding efficacy with excellent safety. There is no potential for antibiotic resistance or off target effects which can occur with tetracycline derivatives and no reported denifanstat-related severe AEs such as hepatotoxicity, hearing impairment and depression which are seen with isotretinoin. Denifanstat should also provide better adherence to treatment compared to topical therapies: an estimated 30% to 40% of patients do not adhere to their topical treatments[1]. Denifanstat is licensed from Sagimet Biosciences Inc. (Nasdaq: SGMT) for exclusive rights in Greater China. "The Phase III clinical trial results for denifanstat are highly encouraging. The data demonstrate statistically significant improvements in treatment outcomes for moderate-to-severe acne patients, with percent treatment success of 33.2%, total lesion count reduction of 57.4% from baseline, inflammatory and non-inflammatory lesion counts decreasing by 63.5% and 51.9%, respectively, while maintaining a favorable safety and tolerability profile. Denifanstat's first-in-class mechanism targeting FASN directly addresses a key cause for acne, establishing it as a groundbreaking therapeutic approach in acne treatment." said Prof. Leihong Xiang, Chief Physician of Dermatological Department, Huashan Hospital, Fudan University, Executive Deputy Director of Institute of Dermatology, Fudan University, Deputy Director of Dermatology Division of Chinese Medical Doctor Association and principal investigator of denifanstat Phase III trial for moderate to severe acne. [1] Purvis CG, Balogh EA, Feldman SR. Clascoterone: How the Novel Androgen Receptor Inhibitor Fits Into the Acne Treatment Paradigm. Ann Pharmacother. 2021;55(10):1297-1299. doi:10.1177/1060028021992055. Table 1. Baseline characteristics of Phase III trial of denifanstat Baseline characteristics 50 mg denifanstat, oral, oncedaily (n=240) Placebo, oral, once daily (n=240) Total lesion count 102.2 102.1 Inflammatory lesion count 42.1 43.1 IGA=3 (moderate), % 85.8 85.8 IGA=4 (severe), % 14.2 14.2 Table 2. Efficacy endpoints of 50 mg denifanstat oral, once daily at week 12 versus placebo (intent-to-treat, ITT, analysis) Efficacy endpoints (1) 50 mg denifanstat, oral, once daily (n=240) Placebo, oral,once daily (n=240) Placebo adjusted p value Percent treatment success (2) (primary endpoint) 33.2 14.6 18.6 <0.0001 Percent reduction from baseline in total lesion count (primary endpoint) 57.4 35.4 22.0 <0.0001 Percent reduction from baseline ininflammatory lesion count (primary endpoint) 63.5 43.2 20.3 <0.0001 Percent reduction from baseline in non-inflammatory lesion count (key secondary endpoint) 51.9 28.9 23.0 <0.0001 Absolute reduction from baseline intotal lesion count (secondary endpoint) 58.3 36.2 22.1 <0.0001 Absolute reduction from baseline in inflammatory lesion count (secondaryendpoint) 26.6 18.4 8.2 <0.0001 Notes: (1) All efficacy endpoints are least square means.(2) Treatment success is defined as an Investigator's Global Assessment (IGA) score of 0 (clear) or 1 (almost clear) with at least a 2-point decrease in IGA from baseline at week 12. 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PR and IR teams+86-181-0650-9129 (China)pr@ ir@ View original content: SOURCE Ascletis Pharma Inc. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

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