Tonix Pharmaceuticals Holding Corp. · NASDAQ:TNXP
Tonix Pharmaceuticals — Investor Presentation (November 2018)
26 slides from Tonix Pharmaceuticals's investor presentation, Nov 1, 2018
Slide 1: Investor Presentation
© 2018 Tonix Pharmaceuticals Holding Corp. November 2018 Version P0141 10 - 31 - 18 (Doc 0404) Investor Presentation
Slide 2: Tonix Development Highlights
© 2018 Tonix Pharmaceuticals Holding Corp. 2 Tonmya ®1 – lead program; FDA Breakthrough Therapy in Posttraumatic Stress Disorder (PTSD) – Bedtime treatment in Phase 3 Development • Results from 2 efficacy studies improve the new Phase 3 study design • Preliminary acceptance of new design features re
Slide 3: Prevalence of PTSD Among Civilians and Veterans
© 2018 Tonix Pharmaceuticals Holding Corp. 3 Prevalence of PTSD Among Civilians and Veterans 1 Goldstein et al., 2016 ; 2 Norris, PTSD Res Quar . 2013; 3 Analysis of VA Health Care Utilization among Operation Enduring Freedom, Operation Iraqi Freedom, and Operation New Dawn Veterans, from 1st Qtr FY
Slide 4: TNX-102 SL Intellectual Property – U.S. Protection until 2034
© 2018 Tonix Pharmaceuticals Holding Corp. 4 TNX - 102 SL Intellectual Property – U.S. Protection until 2034 Composition of matter (eutectic) : Protection expected to 2034 • United States Patent and Trademark Office (USPTO) issued U.S. Patent No. 9,636,408 in May 2017 and U.S. Patent No. 9,956,188 i
Slide 5: Tonmya - Breakthrough Therapy for Treatment of PTSD Targets Sleep Disturbance
© 2018 Tonix Pharmaceuticals Holding Corp. 5 Tonmya® 1 - Breakthrough Therapy for Treatment of PTSD Targets Sleep Disturbance Tonmya - first investigational new drug to show treatment effect in military - related PTSD in two large, 12 - week, multi - center studies Retrospective analyses showed Tonm
Slide 6: Need for Effective and Safe Therapies for Treatment of Military PTSD
© 2018 Tonix Pharmaceuticals Holding Corp. 6 Need for Effective and Safe Therapies for Treatment of Military PTSD PTSD is signature wound of last 25 years of war • Affects servicemember health and performance, force readiness, retention • Believed to be the underlying cause of suicide in many cases
Slide 7: Key Features
© 2018 Tonix Pharmaceuticals Holding Corp. 7 Key Features Tonmya is believed to treat PTSD by improving sleep quality • The brain naturally processes memories during sleep • PTSD sufferers’ emotionally charged memories disturb sleep and disrupt the natural processing of memories during sleep • Tonmy
Slide 8: Tonmya for the Treatment of PTSD
© 2018 Tonix Pharmaceuticals Holding Corp. 8 Tonmya for the Treatment of PTSD One Phase 2 study completed and one Phase 3 study stopped early due to inadequate separation from placebo • Both studies were accepted by the FDA as potential pivotal efficacy studies in military - related PTSD if successf
Slide 9: Tonmya Dose-Effect in Military-Related PTSD
© 2018 Tonix Pharmaceuticals Holding Corp. 9 Tonmya Dose - Effect in Military - Related PTSD 1 1 Phase 2 P201/AtEase study: Retrospective analysis of Tonmya 5.6 mg on CAPS - 5 ≥33 (high - moderate) subgroup. Primary analysis of P 201/AtEase was on Tonmya 2.8 mg in participants with entry CAPS - 5 ≥2
Slide 10: Retrospective Comparison of Time Since Trauma in P201 versus P301
© 2018 Tonix Pharmaceuticals Holding Corp. 10 Retrospective Comparison of Time Since Trauma in P201/AtEase versus P301/HONOR (Tonmya 5.6 mg Groups) P301 study was initiated approximately two years later than Phase 2 P201 • The median time since trauma in Phase 3 was 9.5 years compared to the median
Slide 11: Primary Outcome (CAPS-5) in Phase 3 and ≤9 Years Time Since Trauma Subgroups
© 2018 Tonix Pharmaceuticals Holding Corp. Primary Outcome (CAPS - 5) in Phase 3 ( mITT ) and ≤9 Years Time Since Trauma (TST) Subgroups P301 modified intent to treat ( mITT ) population P301 TST ≤9 yrs ** p=0.004, * p=0.039, # p=0.069, TNX - 102 SL 5.6 mg group v. placebo, using MMRM with MI ~50% m
Slide 12: Sustained Remission in Phase 2 and Phase 3 Studies: Retrospective Analyses
© 2018 Tonix Pharmaceuticals Holding Corp. 12 Sustained Remission in Phase 2 and Phase 3 Studies: Retrospective Analyses of P201 Entry CAPS - 5 ≥33 and P301 ≤9 Years Since Trauma Subgroups Remission is a clinical state that is essentially asymptomatic In order to confirm remission: • Determined rate
Slide 13: Adverse Events in P201/AtEase and P301/HONOR Studies
© 2018 Tonix Pharmaceuticals Holding Corp. 13 Adverse Events (AEs) in P201/AtEase and P301/HONOR Studies No serious and unexpected AEs in P201 or P301 • Systemic AEs comparable between studies and also consistent with those described in approved cyclobenzaprine product labeling • Similar severity an
Slide 14: Summary of Clinical Experience with Tonmya/TNX-102 SL in PTSD
© 2018 Tonix Pharmaceuticals Holding Corp. 14 Summary of Clinical Experience with Tonmya/ TNX - 102 SL in PTSD Median time since trauma (TST) in TNX - 102 SL 5.6 mg group in the P301/HONOR study (9.5 years) was longer than P201/AtEase study (6 years) • Both studied military - related PTSD • Time has
Slide 15: Tonmya/TNX-102 SL – New Phase 3 Study
© 2018 Tonix Pharmaceuticals Holding Corp. 15 Tonmya/TNX - 102 SL – New Phase 3 Study In two prior clinical trials, Tonmya 5.6 mg consistently reduced military - related PTSD severity for participants with ≤ 9 years since trauma These data provide the rationale to study Tonmya’s effect in participan
Slide 16: New Phase 3 P302 Study – To Start 1Q 2019
© 2018 Tonix Pharmaceuticals Holding Corp. 16 New Phase 3 P302 Study – To Start 1Q 2019 Civilian and Military - Related PTSD, ≤9 Years Time since Trauma Primary e ndpoint CAPS - 5 1 : • Mean change from baseline at W eek 4 (Tonmya 5.6 mg vs. placebo ) Key Secondary e ndpoint s include: • CAPS - 5 m
Slide 17: Late-Stage PTSD Drug Candidates
© 2018 Tonix Pharmaceuticals Holding Corp. 17 Late - Stage PTSD Drug Candidates Tonmya • Breakthrough Therapy in Phase 3; only development program focused on military - related and civilian PTSD, only drug to show activity in treatment of military - related PTSD in large multi - center trials MDMA -
Slide 18: TNX-102 SL – Bedtime Treatment for Multiple Potential Indications
© 2018 Tonix Pharmaceuticals Holding Corp. 18 TNX - 102 SL – Bedtime Treatment for Multiple Potential Indications Ma nagement of Fibromyalgia (FM) – chronic pain condition • TNX - 102 SL studied at low dose (2.8 mg) – half the dose being developed for PTSD – did not separate from placebo on primary
Slide 19: TNX-102 SL for Agitation in Alzheimer's – Regulatory Status and Registration Strategy
© 2018 Tonix Pharmaceuticals Holding Corp. 19 TNX - 102 SL for Agitation in Alzheimer’s – Regulatory Status and Registration Strategy FDA confirmed no additional study is needed prior to IND submission • Pre - IND meeting established open dialogue with the FDA on pivotal clinical study design and ef
Slide 20: Candidates in Development
© 2018 Tonix Pharmaceuticals Holding Corp. 20 Candidates in Development Preclinical Phase 2 NDA 1 /BLA 2 Market Pipeline Product Indication/ Description Phase 3 Tonmya Bedtime Treatment for PTSD Daytime Treatment for PTSD TNX - 601 Novel polymorph and salt discovered and characterized; Preliminary h
Slide 21: TNX-601 (Tianeptine Oxalate): A Potential Clinical Candidate for PTSD
© 2018 Tonix Pharmaceuticals Holding Corp. 21 TNX - 601 ( Tianeptine Oxalate): A Potential Clinical Candidate for PTSD Pre - IND Candidate Targeted as a 1 st line monotherapy for PTSD: oral formulation for daytime dosing x Leverages expertise in PTSD (clinical and regulatory experience, market analy
Slide 22: TNX-801 (Synthesized Live Horsepox Virus): A Smallpox-Preventing Vaccine Candidate
© 2018 Tonix Pharmaceuticals Holding Corp. 22 TNX - 801 (Synthesized Live Horsepox Virus): A Smallpox - Preventing Vaccine Candidate Pre - IND Stage Potential improvement over current biodefense tools against smallpox ✓ Leverages Tonix’s government affairs effort ✓ Collaboration with Professor David
Slide 23: Management Team
© 2018 Tonix Pharmaceuticals Holding Corp. 23 Management Team Seth Lederman, MD President & CEO Jessica Morris Chief Operating Officer Gregory Sullivan, MD Chief Medical Officer Bradley Saenger, CPA Chief Financial Officer
Slide 24: Milestones – Recently Completed and Upcoming
© 2018 Tonix Pharmaceuticals Holding Corp. 24 Milestones – Recently Completed and Upcoming □ July 201 8 Completed P301/HONOR study interim analysis - result did not support study continuation but strengthened new Phase 3 study □ August 201 8 Presentation of P301/HONOR study results at Military Healt
Slide 25: Summary
© 2018 Tonix Pharmaceuticals Holding Corp. 25 Summary Phase 3 development of Breakthrough Therapy treatment for PTSD, including military - related PTSD • Major unmet need; ~11 million Americans affected • Benefited from FDA 505(b)(2) NDA approval requirement New indication in development for agitati
Slide 26: Thank you!
© 2018 Tonix Pharmaceuticals Holding Corp. Thank you ! NASDAQ: TNXP
Tonix Pharmaceuticals Holding — Investor Presentation (November 2018) on 6ix