AEVI-001: SAGA Trial in mglur+ ADHD

Similar documents
Deutsche Bank. 42 nd Annual Health Care Conference NASDAQ: GNMX. Mike Cola President & CEO, Aevi Genomic Medicine May 4, 2017

2017 Year-end Results and Corporate Update

Corporate Presentation April 2018

Corporate Update. July, 2018 NASDAQ: GNMX. 2018, Aevi Genomic Medicine

JMP Healthcare Conference June 2018

Piper Jaffray Healthcare Conference. November 30, 2016

Transforming Diagnosis and Treatment Paradigms in Attention Deficit Hyperactivity Disorder (ADHD)

XP23829 PHASE 2 PSORIASIS TRIAL PRELIMINARY TOPLINE DATA PRESENTATION SEPTEMBER 15, 2015 COPYRIGHT 2015 XENOPORT, INC. ALL RIGHTS RESERVED.

Small-Cap Research. Aevi Genomic Medicine (GNMX-NASDAQ) GNMX: SAGA Misses Primary Endpoint But Data-Within-Data Warrants Optimism OUTLOOK SUMMARY DATA

Supernus Pharmaceuticals

JP Morgan. January 2019

JMP Life Sciences Conference. June 2016

Supernus Pharmaceuticals

PROMISE 2 Top-Line Data Results January 8, 2018

Investor Presentation March 2015

STUDY 1 PHASE 3 TOP-LINE RESULTS. September 2017

USPSTF Draft Recommendations Investor Call. October 6, 2015

Investor Presentation. 3 April 2017

PROMISE 1 Top-Line Data Results. June 27, 2017

Keyzilen TM Program Update

35 th Annual J.P. Morgan Healthcare Conference

Alcobra Ltd. (NASDAQ:ADHD) June Dr. Yaron Daniely President & CEO

Committed to Transforming the Treatment Paradigm for Migraine Prevention

Corporate Presentation August 6, 2015

Pimavanserin Top-Line Results Phase III Parkinson s Disease Psychosis Trial (-020 Study) Creating the Next Generation of CNS Drugs

Atomoxetine (First known as Tomoxetine) (Adopted by the CCG until review and further notice)

PATENCY-1 Top-Line Results

ENCORE-PH Top-line Results

For personal use only

-- Single Global Phase 3 Trial Expected to Begin in First Half of

Committed to Transforming the Treatment Paradigm for Migraine Prevention

Alcobra Ltd. (NASDAQ:ADHD) June 2016

Zynerba Pharmaceuticals Announces New FAB-C Phase 2 Open-Label Data in Patients with Fragile X Syndrome

ARDELYX REPORTS POSITIVE T3MPO-2 PHASE 3 TRIAL RESULTS IN IBS-C

SAKURA 3 Open-Label Phase 3 Safety Study with DaxibotulinumtoxinA for Injection (RT002) for the Treatment of Moderate to Severe Glabellar Lines

Capricor Therapeutics

Investor Presentation. 2 June 2017

BRL /RSD-101C0D/1/CPMS-704. Report Synopsis

Neuren s trofinetide successful in proof of concept Phase 2 clinical trial in Fragile X syndrome

Pharmacotherapy of ADHD with Non- Stimulants

Zogenix Announces Positive Top-line Results from Pivotal Phase 3 Clinical Trial of ZX008 in Dravet Syndrome

Zacks Small-Cap Research

Study Center(s): The study was conducted at 39 study sites in Japan.

Study 2 ( ) Pivotal Phase 3 Study Top-Line Results. October 29, 2018

Edasalonexent (CAT-1004) Program

Forward-looking Statements

GLPG1690 FLORA topline results

UCB announces first presentation of primary data from latest Phase 3 study evaluating brivaracetam

The Adolescent with ADHD: Managing Transition

-- Edasalonexent Substantially Slowed Duchenne Muscular Dystrophy Disease Progression through 36 Weeks --

ARCA biopharma. Investment Community Webcast: Top-line Data from GENETIC-AF Phase 2B Clinical Trial

Building a Fully Integrated Biopharmaceutical Company. June 2014

Corporate Presentation Asia Investment Series March 2018

CLINICAL PRIORITIES ADVISORY GROUP 06 and 07 November 2018

Liquid Biopsies. Next Generation Cancer Molecular Diagnostics

Diagnostics for the early detection and prevention of colon cancer. Publication of DeeP-C Study Data in New England Journal of Medicine March 2014

Pioneering Precision Cardiovascular Medicine. (NASDAQ: MYOK) Corporate Presentation March 2018

Phase 2b/3 Topline Trial Results

Rimegepant Pivotal Phase 3 Trial Results - Conference Call March 26, Biohaven

Paliperidone: Clinical Protocol R076477SCH4012, CR Amendment INT-1

Safe Harbor Statement

Diagnostics for the early detection and prevention of colon cancer. Fourth-Quarter 2014 Earnings Call February 24, 2015

SER-287 Phase 1b topline study results in patients with mild-to-moderate Ulcerative Colitis October 2, 2017

- Amendment accelerates anticipated PROSPER top-line results by two years -

Pharmacotherapy of ADHD Across the Lifecycle: Stimulants

Advancing Innovative Therapies for Neurological Diseases

BRL /RSD-101RLL/1/CPMS-716. Report Synopsis

Evercore ISI Presentation- Madrigal

Tonix Pharmaceuticals Reports Top Line Results From Phase 2b BESTFIT Trial of TNX-102 SL in Patients With Fibromyalgia

3/19/2018. Cynthia King, MD Associate Professor of Psychiatry UNMSOM. Autism Spectrum Disorder

3/19/2018. Cynthia King, MD Associate Professor of Psychiatry UNMSOM

Iris Manor, MD. UK Adult ADHD Network 4th Annual Congress London, England September 11, 2014

Corporate Presentation

February 20, 2019 MANAGEMENT CALL TO DISCUSS PHASE 2 PHOENIX RESULTS AND CKD PROGRAM UPDATES

Discovery of Potent, Highly Selective, Broad Spectrum Antivirals

37 th Annual J.P. Morgan Healthcare Conference. January 9, 2019

Role of ADHD medication in children with autism spectrum disorder. Pieter Hoekstra University of Groningen, Netherlands

37 th ANNUAL JP MORGAN HEALTHCARE CONFERENCE

ACTELION S NEW DUAL OREXIN RECEPTOR ANTAGONIST

Summary ID# Clinical Study Summary: Study B4Z-MC-LYBX

AVENUE THERAPEUTICS, INC. NASDAQ: ATXI JANUARY 2018

Is Methylphenidate Transdermal System (Daytrana ) Safe and Effective for Managing Attention Deficit Hyperactivity Disorder Symptoms in Children?

Broad and clinically important benefits beyond the initial registrational endpoints are now reported.

May 10, 2016 Q & Business Update

ASCEND Phase 2 Trial of AXS-05 in MDD Topline Results Conference Call

Pharmacotherapy of ADHD with Non-Stimulants

NASDAQ: ZGNX. Company Presentation. October 2017

Piecing the Puzzle Together: Pharmacologic Approaches to Behavioral Management in Autism Spectrum Disorder

The difficulties in going from P2 to P3 in CNS trials Red flags from a recent CIS program. ISCTM February 2017

I.V. CR845 Adaptive Phase 2/3 Post Operative Pain Study Results

XanADu: A Phase II trial of Xanamem TM in mild Alzheimer's disease

BioArctic announces positive topline results of BAN2401 Phase 2b at 18 months in early Alzheimer s Disease

First US Plan to Address Alzheimer s Disease

Corporate Overview June 2014 Jefferies Healthcare Conference NASDAQ: GLYC

Two late stage clinical programs

SYNOPSIS. Risperidone-R064766: Clinical Study Report RIS-USA-232 (FOR NATIONAL AUTHORITY USE ONLY)

Acorda Acquisition of Civitas Therapeutics. September 24, 2014

Creating a Leading Global HBV Therapeutics Company. ARB-1467 Update Call December 12, 2016

Advancing New Treatments for DMD and C. difficile Infection

Transcription:

AEVI-001: SAGA Trial in mglur+ ADHD Topline Results March 20, 2017 2017, Aevi Genomic Medicine

Forward-Looking Statement This presentation includes certain estimates and other forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, including statements with respect to anticipated operating and financial performance, clinical results, potential partnerships, licensing opportunities and other statements of expectation. Words such as expects, anticipates, intends, plans, believes, assumes, seeks, estimates, should and variations of these words and similar expressions, are intended to identify these forward-looking statements. While we believe these statements are accurate, forward-looking statements are inherently uncertain and we cannot assure you that these expectations will occur and our actual results may be significantly different. These statements by the Company and its management are based on estimates, projections, beliefs and assumptions of management and are not guarantees of future performance. Important factors that could cause actual results to differ from those in the forward-looking statements include the factors described in the Company s filings with the U.S. Securities and Exchange Commission. The Company disclaims any obligation to update or revise any forward-looking statement based on the occurrence of future events, the receipt of new information, or otherwise. 2017, Aevi Genomic Medicine 2

SAGA Trial Summary Trial did not meet primary endpoint (overall ADHD-RS) 1, however showed encouraging trend in improvement at highest dose (400 mg BID) Strong trend of efficacy in ADHD-RS inattention subscale (p=0.0515 vs placebo) Clear signal of efficacy and benefit to patients ADHD-RS response rate 2 70% (p=0.0067 vs placebo) CGI-I response rate 3 57% (p=0.0155 vs placebo) Well tolerated with no serious AEs 1. ADHD-RS: parent reported scale on hyperactivity and inattention, 18 questions; scored 0-3 2. Pre-specified endpoint, response defined as improvements in ADHD-RS scores of > 30% 3. Pre-specified endpoint, response defined as much or very much improved (CGI-I of 1 or 2) 2017, Aevi Genomic Medicine 3

A Novel Paradigm of Diagnosis and Treatment in Neuropsychiatric Diseases Novel genomic discovery identifies disruptive mutations in the mglur network in a significant subpopulation (20-25%) of ADHD patients Role of glutamate in ADHD is supported by recent genetic 1 and neuroimaging 2,3 findings Highly predictive biomarker facilitates precision medicine approach mglur network mutations also found in other neurodevelopmental disorders 22q deletion syndrome Autism spectrum disorder Pediatric anxiety disorder AEVI-001 identified as a promising targeted therapeutic for mglur+ patients 1. Elia et al. (2012) Nat Genet, 44(1):78-84 2. Gallo and Posner (2016) Lancet Psychiatry, 3(6):555-67. 3. Spencer et al. (2014) J Clin Psychiatry;75(11):1226-412 2017, Aevi Genomic Medicine 4

AEVI-001 A glutamate signaling modulator Oral non-stimulant Originator: Nippon Shinyaku MOA: Pan-selective activator/modulator of mglurs that modulates glutamatergic signaling restoring homeostasis 1,2 Excellent PK/metabolic profile O H N O N Crosses blood-brain barrier 3,4,5 Comprehensive pre-clinical toxicology package Prior human exposure: ~1000 elderly patients with vascular dementia, up to 12 months Efficacy signal in 30 adolescent ADHD patients (GREAT Trial) Excellent safety profile 1. Oka et al. (1997) Naunyn Schmiedebergs Arch. Pharmacol, 356(2): 189. 2. Hirouchi et al. (2000) Eur J Pharmacol, 387(1):9-17. 3. Ogasawara et al. (1999) Pharmacol Biochem Behav, 64(1):41-52. 4. Nakagawa et al. (1988) Jpn J Pharmacol, 46(Suppl.): Abst O-258. 5. Nakagawa et al. (1990) Jpn J Pharmacol, 52(Suppl. I): Abst P-491. 2017, Aevi Genomic Medicine 5

SAGA Trial Design in mglur+ Adolescents Multicenter (24 sites) Inclusion criteria: Adolescents (12-17 years of age) ADHD-RS-5 28 Positive for mglur mutation Investigators, patients and parents were not blinded to genetic status Primary endpoint: ADHD-RS-5 Key secondary endpoint: CGI-I 1:1 randomization Placebo-controlled Dose optimization: 100-400 mg BID *Elia et al. (2012) Nat Genet, 44(1):78-84 2017, Aevi Genomic Medicine 6

Patient Demographics Age Parameter AEVI-001 (n=46) Placebo (n=50) Mean (SD) 13.8 (1.40) 14.4 (1.68) Gender Male Female 26 (55%) 20 (45%) 35 (70%) 15 (30%) ADHD-RS-5 Total Score at Baseline Mean (SD) 36.8 (6.88) 38.6 (7.23) CGI-S Score at Baseline Mean (SD) 4-Moderate (N, %) 5-Marked (N, %) 6-Severe (N, %) Treatment History Stimulants Non-stimulants Atypicals 4.43 (0.54) 28 (60%) 18 (38%) 1 (2%) 31 (67%) 3 (7%) 0 (0%) 4.38 (0.49) 31 (62%) 19 (38%) 0 (0%) 36 (72%) 3 (6%) 1 (2%) 2017, Aevi Genomic Medicine 7

Change in ADHD-RS Score from Baseline Over Time Parent reported scale on inattention and hyperactivity No statistically significant reduction in ADHD symptoms between treatment and placebo 20% of patients on AEVI-001 had no appreciable reduction in ADHD-RS ( 3) Opportunity to enrich for responders using genomic biomarker Trend in improvement vs placebo starting at Week 4; 88% of patients reached 400 mg BID Opportunity to increase effect size with higher doses and/or longer exposure in future studies Adolescent ADHD studies generally have lower effect size than pediatrics Recently completed PK and toxicology studies will enable pediatric trials and higher dosages Change in ADHD-RS Score from Baseline 0-5 -10-15 -20 Baseline Week 1 (100 mg BID) Week 2 (200 mg BID) Week 3 (400 mg BID) Week 4 (Optimized Dose) Week 5 (Maintenance Dose) Week 6 (Maintenance Dose) Placebo AEVI-001 p=ns ADHD-RS: parent reported scale on hyperactivity and inattention, 18 questions; scored 0-3 2017, Aevi Genomic Medicine 8

Clinically and Statistically Significant Response Rate (ADHD-RS Reduction > 30%) Significantly more treated patients were responders as measured by ADHD-RS* 70% response rate in treatment arm vs 42% in placebo arm (p=0.0067) at Week 6 Concerta achieved a response rate of 73.3% in an adolescent ADHD study 1 Results warrant consideration of higher doses and/or longer exposure in future studies Percentage of patients who achieved reduction in ADHD-RS > 30% 80 60 40 20 0 Week 1 (100 mg BID) Week 2 (200 mg BID) Week 3 (400 mg BID) Week 4 (Optimized Dose) p=0.0203 Week 5 (Maintenance Dose) p=0.0067 Week 6 (Maintenance Dose) AEVI-001 Placebo 1. Wilens et al. (2006) Arch Pediatr Adolesc Med. 160(1):82-90 * Pre-specified endpoint, response defined as improvements in ADHD-RS scores of > 30% 2017, Aevi Genomic Medicine 9

Clinically and Statistically Significant Response (CGI-I of 1 or 2) at Week 6 CGI-I is the physicians assessment of the change in patient s overall illness, including co-morbidities 57% response rate* in treatment arm vs 33% in placebo arm (p=0.0155) at Week 6 Concerta achieved a response rate of 51.8% in an adolescent ADHD study 1 Intuniv achieved a response rate of 55% in ADHD patients ages 6-17 2 Results warrant consideration of higher doses and/or longer exposure in future studies Percentage of patients who achieved CGI-I of 1 or 2 60 40 20 0 Week 1 (100 mg BID) Week 2 (200 mg BID) Week 3 (400 mg BID) Week 4 (Optimized Dose) Week 5 (Maintenance Dose) p=0.0155 Week 6 (Maintenance Dose) AEVI-001 Placebo 1. Wilens et al. (2006) Arch Pediatr Adolesc Med. 160(1):82-90 2. Biederman et al. (2008) Pediatrics. 121(1):e73-84 CGI-I: 7-point scale assessing patients improvement or worsening of illness *Pre-specified endpoint, response defined as much or very much improved (CGI-I of 1 or 2) 2017, Aevi Genomic Medicine 10

AEVI-001: Safety and Tolerability AEVI-001 was well-tolerated; 88% achieved highest dose of 400 mg BID No serious adverse events Majority of AEs judged to be mild or moderate AEVI-001 Placebo Number of subjects with 1 AE 33/47 (70.2%) 28/50 (56%) AEs > 5% Weight gain Fatigue Headache Nausea 7 (14.9%) 7 (14.9%) 4 (8.5%) 3 (6.4%) 2 (4%) 3 (6%) 5 (10%) 4 (8%) 2017, Aevi Genomic Medicine 11

AEVI-001: Next Steps Enrich ADHD study population to enhance response rate and effect size: Refine responders using genomic biomarker Higher exposure: dose and duration Pediatric (ages 6-12) ADHD study: Higher responses, better compliance, lower placebo effect Additional signal finding studies planned in: Autism spectrum disorder Pediatric anxiety disorder FDA meeting planned mid-2017 Development plan including companion diagnostic Full data to be presented at World Congress on ADHD (April 20-23, Vancouver, Canada) 2017, Aevi Genomic Medicine 12

Thank you 2017, Aevi Genomic Medicine 13