Developing Therapeutics for the Treatment of Serious Rare and Life-Threatening Diseases with Critical Unmet Medical Needs Corporate Presentation August 13, 2019 Nasdaq: ACER Exhibit 99.2

Forward-looking Statements This presentation contains “forward-looking statements” that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. All statements, other than statements of historical facts, included in this presentation regarding strategy, future operations, future financial position, future revenues, projected expenses, regulatory actions or approvals, cash position, liquidity, prospects, plans and objectives of management are forward-looking statements. Examples of such statements include, but are not limited to, statements relating to expectations regarding our capital resources; the anticipated future reduction in operating and cash conservation benefits associated with our corporate restructuring initiative; the potential for EDSIVO™ (celiprolol), ACER-001, and osanetant to safely and effectively treat diseases and to be approved for marketing; the commercial or market opportunity of any of our product candidates in any target indication; the adequacy of our capital to support our future operations and our ability to successfully initiate and complete clinical trials and regulatory submissions; our progress toward possible approval for EDSIVO™ and our other product candidates; the ability to protect our intellectual property rights; our strategy and business focus; and the development, expected timeline and commercial potential of any of our product candidates. We may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Such statements are based on management’s current expectations and involve risks and uncertainties. Actual results and performance could differ materially from those projected in the forward-looking statements as a result of many factors, including, without limitation, risks and uncertainties associated with the ability to project future cash utilization and reserves needed for contingent future liabilities and business operations, our ability to reduce our operating expenses and conserve cash on a net basis as a result of our prior or any future corporate restructuring initiative, the availability of sufficient resources to meet our business objectives and operational requirements, the fact that the results of earlier studies and trials may not be predictive of future clinical trial results, the protection and market exclusivity provided by our intellectual property, the substantial costs and diversion of management’s attention and resources which could result from securities class action litigation, risks related to the drug development and the regulatory approval process, including the timing of regulatory actions, and the impact of competitive products and technological changes. We disclaim any intent or obligation to update these forward-looking statements to reflect events or circumstances that exist after the date on which they were made. You should review additional disclosures we make in our filings with the Securities and Exchange Commission, including our Quarterly Reports on Form 10-Q and our Annual Report on Form 10-K. You may access these documents for no charge at http://www.sec.gov.

Corporate Overview Acer Therapeutics is a pharmaceutical company that acquires, develops and seeks to commercialize therapies for serious rare and life-threatening diseases with critical unmet medical needs Headquartered: Newton, MA Headcount: 19 Founded: December 2013 Public: September 2017 Cash: $23.5M as of June 30, 2019 Expected to have sufficient capital through end of 2020 ACER

Executive Leadership Team Chris Schelling CEO & Founder 20 years; strategic commercial development & orphan Will Andrews, MD Chief Medical Officer 20 years; clinical development, medical affairs & orphan M.D. Yale University School of Medicine Matt Seibt Interim Head of Commercial 22 years; sales, market access & product launch Harry Palmin Chief Operating & Financial Officer 25 years; corporate & finance experience Don Joseph, JD Chief Legal Officer & Secretary 25 years; general counsel & senior management J.D. University of Texas School of Law ACER Biomarin Sunovion Biogen Novelos bvgh BIO Ventures for Global Health

Investment Highlights Acer’s pipeline includes three clinical-stage product candidates: EDSIVO™ (celiprolol) for the treatment of vascular Ehlers-Danlos syndrome (vEDS) in patients with a confirmed type III collagen (COL3A1) mutation ACER-001 (a fully taste-masked, immediate release formulation of sodium phenylbutyrate) for the treatment of various inborn errors of metabolism, including urea cycle disorders (UCDs) and Maple Syrup Urine Disease (MSUD) Osanetant for the treatment of induced Vasomotor Symptoms (iVMS) where Hormone Replacement Therapy (HRT) is likely contraindicated Acer’s product candidates are believed to present a comparatively de-risked profile, having one or more of: Favorable safety profile; Clinical proof-of-concept data; Mechanistic differentiation Accelerated paths for development through specific FDA-established programs Multiple anticipated key regulatory milestones: EDSIVO™ Type A mtg w/FDA:Q3 2019 ACER-001 (UCD) pivotal bridging & taste assessment trials initiation:Q4 2019 Osanetant IND submission:Q4 2019 ACER-001 (UCD) NDA submission*:Mid-2020 Osanetant Phase 1/2 PK/PD/safety trial initiation**:Mid-2020 Expected to have sufficient capital through end of 2020 ACER * Assuming successful outcomes in bridging trials and NDA submission with 6 months stability data ** Subject to additional capital

Program / Indication Novel MOA / Unique Characteristics Phase 1 Phase 2 Phase 3 NDA Market EDSIVOTM (celiprolol) vascular Ehlers-Danlos syndrome (COL3A1+)* Induces vascular dilatation and smooth muscle relaxation ACER-001 (reformulated sodium phenylbutyrate) Urea Cycle Disorders Taste-masked formulation; evaluating comparability to Buphenyl® Maple Syrup Urine Disease Inhibition of BCKD kinase to increase BCAA metabolism Osanetant Induced Vasomotor Symptoms (iVMS) Neurokinin 3 Receptor Antagonist Clinical Pipeline ACER * CRL received after market close 6/24/19

EDSIVO™ has a unique pharmacological profile β2 and β3 adrenergic receptor agonist; selective β1 and ⍺2 adrenergic receptor antagonist; activates endothelial Nitric Oxide Synthase (eNOS) EDSIVO’s™ potential beneficial effects in vEDS thought to be through vasodilation and vascular smooth muscle dilation, thereby reducing the mechanical stress on collagen fibers within the arterial wall. Mechanism of Action No approved therapeutic options for vEDS patients Autosomal dominant connective tissue disorder of collagen synthesis caused by mutations in the COL3A1 gene for type III procollagen Characterized by arterial aneurysms, dissections and/or ruptures Median survival in the U.S. is estimated to be 51 years of age Disease Overview FDA CRL received after market close June 24; conduct Type A meeting in Q3 2019 Corporate restructuring initiative implemented and pre-commercial activities of EDSIVO™ halted Seeking viable path forward with FDA which may include Formal Dispute Resolution Request The Opportunity BBEST Pivotal trial: 64% reduction in risk of arterial events observed1 Statistically-significant improvement in event-free survival (EFS) compared to control in vEDS patients (n=53)1 17-year vEDS long-term observational study (n=144) published in JACC2 Product Profile EDSIVO™ EDSIVO™ Overview 1. Ong Lancet 2010; 376: 1476-84. 2. Frank et al., J Am Coll Cardiol. 2019 Apr 23;73(15):1948-1957.

Received CRL from FDA on June 24, 2019 stating that it will be necessary to conduct an adequate and well-controlled trial to determine whether celiprolol reduces the risk of clinical events in patients with vEDS Following receipt of CRL, corporate restructuring implemented to reduce operating expenses and conserve cash, and pre-commercial activities of EDSIVO™ halted Acer is working with Hyman, Phelps, & McNamara (HPM) and other leading industry experts to determine the optimal path forward Continue to work toward our goal of approval of EDSIVO™ for confirmed COL3A1+ vEDS patients EDSIVO™ EDSIVO™: CRL and Next Steps

In 2016, FDA published that from 2003-2014, of the 140 appeals accepted, 16% were granted and 84% denied. According to HPM, these “denials” are most often “wins” While approval is not provided based on the previous NDA submission, the company is given a more favorable path forward to approval than was presented in the CRL Between 2015-2018, HPM worked on 9 appeals FDA counted these as 12 appeals, and granted 3 (25%) HPM describes that 7 of the 9 cases were given a more favorable alternative path to approval than outlined in the review (78%) The results of prior appeals, as well as any appeal involving a program other than EDSIVO™, should not be viewed as predictive of any appeal involving EDSIVO™ EDSIVO™ EDSIVO™: CRL and Next Steps http://www.fdalawblog.net/2018/10/formal-dispute-resolution-a-different-perspective-on-wins-and-losses-2/

Conduct a Type A meeting with FDA to make sure we fully understand FDA’s thought process for the CRL Depending on outcome, consider submission of a Formal Dispute Resolution Request (FDRR) Depending on issues and outcomes, we may be able to resubmit our NDA, but no assurances The entire process will likely take many months and possibly a year or more to reach final outcome We will provide updates as appropriate and may discontinue the process at any point where risk/benefit no longer justifies continued resources EDSIVO™ EDSIVO™: CRL and Next Steps

Ehlers-Danlos syndrome (EDS) is a group of hereditary disorders of connective tissue vEDS (EDS type IV) is the severe subtype: Characterized by aneurysms, dissections and/or ruptures Vascular Gastrointestinal Uterine Autosomal dominant (50%); spontaneous mutations (50%) Diagnosed by clinical symptoms and confirmed by presence of mutations in the COL3A1 gene Events occur in 25% of patients before the age of 20, but 90% by the age of 40 Median age of death is estimated to be 51 years1 No approved therapeutic options for vEDS Current treatment is focused on surgical intervention Fig. 3 Distribution of 132 vascular complications in 24 patients with a clinical diagnosis of EDS type IV. J Vasc Surg 2005;42:98-106. 1 Pepin Genet Med. 2014 Dec;16(12):881-8. EDSIVO™ Vascular Ehlers-Danlos Syndrome (vEDS) Cerebral (3) Vertebral (2) Subclavian (8) Axillary (2) Thoracic aorta (10) Splenic (5) Renal (9) IMA (1) Iliac (9) SFA (3) Tibial (1) Carotid (8) Innominate (5) Arch (6) Celiac (4) Hepatic (4) SMA (6) Ileocolic (1) Abdominal aorta (7) Femoral (8) Popliteal (4) n = 24 patients 132 complications

Cardiology in Review 2017;25: 247–253. * Hypertension 2003 Nov;42(5):1004-13. EDSIVO™ has a unique pharmacological profile: β2 and β3 adrenergic receptor agonist Selective β1 and ⍺2 adrenergic receptor antagonist Intrinsic sympathomimetic activity (ISA+) Lacks non-specific membrane effects Activates endothelial Nitric Oxide Synthase (eNOS)* Void of blood pressure lowering in normotensive people Most vEDS patients are normotensive, thus the potential beneficial effect of celiprolol is unlikely to be through blood pressure lowering (β1 antagonism) EDSIVO’s™ potential beneficial effects in vEDS patients are thought to be through vasodilation and vascular smooth muscle dilation, thereby reducing the mechanical stress on collagen fibers within the arterial wall. EDSIVO™ Unique Mechanism of Action Carvedilol (α1) With α-antagonism Labetalol (α1) Celiprolol (α2) Non-selective β-adrenoceptor antagonists Atenolol Bisoprolol Betaxolol Metoprolol Esmolol Nebivolol Negative ISA β1-Selective β-adrenoceptor antagonists Positive ISA Vasodilating Property Without Vasodilating Property Acebutolol Carteolol Penbutolol Propranolol Sotalol Nadolol Timolol Pindolol Oxprenolol Non-selective

Efficacy: 64% reduction in the average risk of fatal or nonfatal cardiac or arterial events in EDSIVO™ patients vs. control group over mean follow-up of 47 months 76% average reduction in risk of fatal or nonfatal cardiac or arterial events in COL3A1+ EDSIVO™ patients vs. control group Trial stopped early for clinical benefit (mean follow-up 47 months) Significant differences in treatment effect were observed; consensus decision of DSMB, statisticians and principal investigator Primary Endpoint Primary + Secondary Endpoints Ong Lancet 2010; 376: 1476-84. 0 12 24 36 48 60 72 EDSIVO™ BBEST Pivotal Clinical Trial Primary Endpoint Proportion of survival free events (%) 0 25 50 75 100 A 12 24 36 38 60 72 p=0.400 Celiprolol Control Number at risk/events 28 24/2 21/5 16/5 13/5 5/5 27/2 22/7 15/11 7/14 5/14 B Primary + Secondary Endpoints 23/3 30/6 16/6 13/6 5/6 24/5 16/13 10/16 6/17 4/17 Figure 2: Kaplan-Meier curves of event-free survival in 53 patients with vascular Ehlers-Danlos Primary endpoint (A). Primary and secondary endpoints (b). P=0.0097 Time (months)

Efficacy: Between 2000 and 2017, 144 patients (median age at diagnosis 34.5 years; 100% COL3A1+) were included in this study (A) Patients not treated with celiprolol had a significantly worse survival outcome than treated patients: Overall survival was 80.7% (95% CI: 67.8% to 93.6%) in those treated with celiprolol (n = 110) versus 48.5% (95% CI: 19.7% to 77.4%) in those not treated (n = 22) after 11.1 years of follow-up: p = 0.0002 (B) Survival was significantly improved in patients taking celiprolol 400 mg/day compared with patients taking lower doses, suggesting a dose effect and that 400 mg/day should be considered the optimal treatment dose: At the end of follow-up, survival was 85% (95% CI: 70.5% to 99.5%) in those patients treated with celiprolol 400 mg/day and 69.2% (95% CI: 41.4% to 97.0%) in those taking celiprolol 100 to 300 mg/day: p = 0.035 Statistically significant reduction in rate of hospitalization for acute arterial events after systematic introduction of celiprolol treatment Frank et al., J Am Coll Cardiol. 2019 Apr 23;73(15):1948-1957. EDSIVO™ Long-Term Observational Study FIGURE 3 Kaplan-Meier Survival Analysis of vEDS Patients in Groups I and II COL3A1 Pathogenic Variants, According to Celiprolol Treatment A B Proportion Still living Log Rank p = 0.0002 Follow-Up (Year) Others Treated by Celiprolol p = 0.035 400 mg/day <400 mg/day 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100% 0 2 4 6 8 10 12 14 16 18 20 22

EDSIVO™ U.S. vs. French vEDS Patients Pepin Genet Med. 2014 Dec;16(12):881-8. Frank et al., J Am Coll Cardiol. 2019 Apr 23;73(15):1948-1957. Median Survival: 51 years (46 y.o. males; 54 y.o. females) U.S. vEDS Natural History 1,231 patients (>90% COL3A1+; 630 index / 601 relatives) French vEDS Population 144 patients (100% COL3A1+; 91 index / 53 relatives) Median Survival: Not Met US all US females US males vEDS females vEDS males vEDS all Proportion still living Last known age in years French General Population Treated with Celiprolol Vascular Ehlers-Danlos Syndrome Patients Not Treated Last Known Age (Year) 0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100

Background: No currently approved medications to treat vEDS There is no evidence supporting the use of antihypertensive medications in vEDS Methods: Retrospective analysis of U.S. insurance claims identifying vEDS patients 2014-2017 Patient data stratified based on claims for patients taking antihypertensive medications and not taking an antihypertensive medication Calculated and compared clinical event rates for each group Results: Study suggests that minority of U.S. vEDS patients (34%) are being treated with antihypertensive medications Data showed no significant difference in clinical event rates in U.S. patients taking antihypertensive medications (16.5%) vs. those not taking an antihypertensive (15.6%) medication Underscores need for an effective treatment Tetali et al. Poster Presentation: Pilot Study to Evaluate Effect of Antihypertensive Therapy on the Rates of Clinical Events in Patients with Vascular Ehlers-Danlos Syndrome. Society for Vascular Medicine 2019 Annual Scientific Sessions, May 30, 2019 EDSIVO™ SVM Poster: Antihypertensive Therapy Table 4. Rate of Clinical Events in vEDS Patients on Antihypertensive Therapy vEDS Patient Group No. Patients (%) Rate of Clinical Events P-value (vs. No Antihypertensive) No antihypertension therapy 2,371 (65.6%) 271 (15.6%) – Any antihypertension therapy 1,243 (34.4%) 205 (16.5%) 0.51 Beta blocker 895 (24.8%) 146 (16.3%) 0.64 ACE inhibitor 231 (6.4%) 38 (16.5%) 0.75 ARB 228 (6.3%) 55 (24.1%) 0.999 Calcium channel blocker 254 (7.0%) 33 (13.0%) 0.27

Small molecule with unique MOAs in various disorders UCDs: NaPB is a prodrug of phenylacetate, a NH4+ scavenger MSUD: NaPB is an allosteric inhibitor of BCKD kinase UCDs: A group of metabolic genetic diseases that lead to toxic build-up of NH4+ UCDs: Currently treated with Ravicti, Buphenyl, Ammonul, and a highly-restricted diet MSUD: A metabolic genetic disease that leads to toxic build-up of leucine and other branched-chain amino acids MSUD: Currently managed with a highly-restricted diet; poor compliance Anticipate NDA submission for UCD mid-2020* UCDs: >2,000 patients in the U.S.; ~600 patients treated with sodium / glycerol phenylbutyrate MSUD: ~800 eligible patients in the U.S. Advantageous orphan pricing with robust program to support patient access and reimbursement A taste-masked, immediate release formulation of sodium phenylbutyrate UCDs: Will conduct a PK/BE study to show bioequivalence to Buphenyl MSUD: POC study suggests ~60% of patients have 30% reduction in Leucine ACER-001 Mechanism of Action Disease Overview The Opportunity Product Profile ACER-001: Overview * Assumes Acer NDA submission with 6 months drug product stability data

Newborns with severe urea cycle disorders become catastrophically ill with symptoms that mimic sepsis -- failure to feed, lethargy, respiratory distress, seizures and ultimately coma Children and adults with milder (or partial) urea cycle enzyme deficiencies may go years without a diagnosis, until a trigger -- a high protein meal, viral illness, excessive exercise or calorie deficiency -- causes excessive ammonia to be produced in the body, resulting in critical elevations of blood ammonia levels For individuals with OTC deficiency, typical neuropsychological complications include developmental delay, learning disabilities, intellectual disability, attention deficit hyperactivity disorder (ADHD), and executive function deficits ACER-001 UCDs: Clinical Manifestations Ah Mew N, et al.. Urea cycle disorders overview. Gene Reviews. Seattle, Washington: University of Washington, Seattle; 1993. Lichter-Knoecki U., et al. Ornithine Transcarbamylase Deficiency, Gene Reviews. Seattle, Washington: University of Washington, Seattle; 1993-2019. Reproduced from:   http://upload.wikimedia.org/wikipedia/commons/7/76/Symptoms_of_hyperammonemia.svg. Symptoms of Hyperammonemia General – Growth retardation – Hypothermia Central – Combativeness – Lethargy – Coma Eyes – Papilledema Muscular/Neurologic – Poor coordination – Dysdiadochokinesia – Hypotonia or hypertonia - Ataxia – Tremor – Seizures – Decorticate or decerebrate posturing Pulmonary – Shortness of breath Liver – Enlarge-ment

ACER-001 UCDs: Unmet Need Buphenyl®: Foul odor and foul/bitter taste; considered unpalatable* 64% of patients reported it is difficult to take because of taste Physicians reported that 25-33% of patients were prescribed less than target dose due to tolerability Only 25% of patients indicated that they never miss a dose 46% of patients reported taste as the reason for discontinuation* Ravicti®: Tasteless/Odorless Pricing has risen to levels considered challenging Reports of difficult access, unaffordability, and forced switches back to sodium phenylbutyrate (NaPB) For example: Buphenyl® and Ravicti® both recently removed from CVS/Caremark formulary for JPMorgan Chase plan members, effective 8/1/2019** Patient groups and physicians have called for a taste-masked, affordable and accessible treatment*** * Shchelochkov et al., Barriers to drug adherence in the treatment of urea cycle disorders: Assessment of patient, caregiver, and provider perspectives. Molecular Genetics and Metabolism Reports 8 (2016) 43-47. ** https://www.caremark.com/portal/asset/Formulary_Drug_Removals_JPMC.pdf *** Acer Market Research

Mouth → Stomach Protection for several minutes at mouth pH followed by rapid release at stomach pH ACER-001 ACER-001: Taste-masked, IR Formulation TM coat (Eudragit E) Seal coat (HPMC) Drug layer (NaPB, HPMC) Seed core (microcrystalline cellulose) Expected drug loading maximum ~50% ~400µm Drug Layered Core % drug dissolved Time (min) pH 6.8 – 1.2 pH change 0 10 20 30 40 50 60 80 100

Phenylbutyrate Formulations ACER-001* RAVICTI® BUPHENYL® Efficacy / Safety in UCDs ✓ ✓ ✓ Palatability / Compliance ✓ ✓ ✘ ** Pricing (Per Patient Per Year) TBD, likely near BUPHENYL $158k-$1.2M*** $204k-$402k*** Formulation Multi-Particulate Beads (Sachet) Oil (Tablespoons) Powder/Tablets (up to 40 tablets/day) Indication all ages  ✓ ✓ ✓  * Subject to FDA Approval ** Molecular Genetics & Metabolism Reports 8 (2016) 43-47 *** Ravicti & Buphenyl pppy is based on patient weight and WAC price ACER-001 ACER-001: Differentiation

ACER-001 IND: active as of May 31st, 2019 Pivotal bridging trial: initiation expected Q4 2019 Stage 1: comparison of three formulations of ACER-001 in healthy adult subjects to select optimal formulation Stage 2: single-dose, fasting, comparative bioequivalence study in healthy adult subjects to establish the bioequivalence of ACER-001 to sodium phenylbutyrate Up to 64 healthy volunteers Multiple-day trial 1 dose of sodium phenylbutyrate, 1 dose of ACER-001 Taste assessment trial: initiation expected Q4 2019 Comparing ACER-001 to sodium phenylbutyrate in healthy subjects NDA: anticipate submitting mid-2020* pending successful outcome of bridging trials and Type C Meeting with FDA ACER-001 UCDs: Clinical & Regulatory Path * Assumes Acer NDA submission with 6 months drug product stability data

UCDs: Market Opportunity Target existing Rx market share in UCDs Currently 1,100 patients diagnosed with ~600 patients on Rx therapy* 2018 U.S. Revenue for Ravicti® & Buphenyl® = $248.4M   Goal: transition patients from Ravicti® & Buphenyl® to ACER-001 and capture a portion of new UCD Rx “Transition” Value Story: A cost-effective, taste masked alternative for UCDs (assuming successful studies and FDA approval): Bioequivalence to sodium phenylbutyrate  Greater compliance/adherence compared to Buphenyl® expected due to differentiated formulation providing taste masked alternative Competitively priced vs Ravicti®  Payer engagement strategy to support switching ACER-001 * https://www.sec.gov/Archives/edgar/data/1386858/000119312515110284/d899054dex992.htm (HZNP IR Presentation)

MSUD is an inborn error of Branched-chain Amino Acid (BCAA) – leucine, isoleucine, valine – metabolism Caused by deficiency of the mitochondrial Branched-chain Keto Acid Dehydrogenase complex (BCKDC) ~800 patients in U.S., ~3,000 patients worldwide MSUD Family Support Group has >500 patients Part of newborn screening in U.S., UK, Germany High leucine levels lead to chronic and acute neurological damage Lower IQ Mental impairment (poor cognitive function) Social impairment (poor executive function) Metabolic decompensation (seizures and coma) A highly-restricted diet is the primary treatment Consists of BCAA-free synthetic foods and formula Very few foods have low BCAAs (fruits & vegetables) Balancing act: enough BCAAs for growth & development indicates p < 0.05, *** p < 0.001 compared to the control group* * Muelly 2011 Neuropsychiatric and Neurochemical Sequelae of MSUD. ACER-001 Maple Syrup Urine Disease (MSUD) Full Scale IQ 60 80 100 120 140 40 50 70 90 0 5 10 15 20 25 A B C D Conner’s Parent Rating Scale SDM-IV ADHD Symptoms Hamilton Anxiety Score Hamilton Depression Score Controls MSUD

ACER-001 MSUD: Clinical POC Study Design: Open label pilot study1 at BCM – 3 healthy and 5 MSUD subjects with late onset disease 3 days of steady-state protein diet*; then 3 days of NaPB + diet* BCAAs and BCKAs determined at day 3 of each study period (4 time points) Results: NaPB demonstrated statistically significant leucine reduction in all 3 healthy subjects (p< 0.05) and 3 out of 5 MSUD patients (p< 0.05 in responders) ~30% reduction (28-34%) in leucine in MSUD responders Clinicians view >20-30% ↓ as clinically meaningful** Comments: Despite the short treatment duration (3 days) NaPB showed statistically significant (intra-subject) reduction in leucine in 75% of the subjects Brunetti-Pierri et al., Hum Mol Genet. 2011 February 15; 20(4): 631–640 1 Brunetti-Pierri et al., Hum Mol Genet. 2011 February 15; 20(4): 631–640 * All subjects received a constant protein intake of 0.6 g/kg/day as combination of BCAA-free formula and whole protein ** Acer commissioned market research Healthy Subjects (n=3) MSUD Subjects (n=5) Total (n=8)

MSUD: Market Opportunity About 1,000 MSUD patients in the U.S., ~3,000 WW 20-25% MSUD patients in U.S. are Mennonite; incidence up to 1/380 Ashkenazi Jewish population; incidence of 1/26,000 No treatments currently approved for MSUD ACER-001 granted U.S. Orphan Drug status by FDA Early treatment may help reduce the rate of neuropsychological comorbidities and optimize growth* MSUD specialists recognize NaPB’s potential effectiveness, yet tolerability is a concern** ACER-001 taste masked formulation may provide much needed treatment option Anticipate initiating Phase 2 trial in MSUD mid-2020, subject to additional capital ACER-001  * Molecular Genetics and Metabolism Reports 15 (2018) ** Acer Therapeutics: US Market Research – 2014

ACER-001 ACER-001: Exclusivity / IP Filed formulation and method of use patent application (filed Oct. 2016) Issued patents (US/EP): “Methods of modulation of branched chain acids and uses thereof” [US PATENT NO. 10,092,532] Exclusive license rights from Baylor College of Medicine UCDs: 505(b)(2) application: 3 years market exclusivity from FDA approval (pending feedback from Type C Meeting) MSUD: Granted U.S. Orphan Drug Designation: 7 years market exclusivity from FDA approval Pediatric exclusivity: +6 months added (if pediatric indication study approved)

Osanetant is a selective, non-peptide tachykinin NK3 receptor antagonist NK3R is the main receptor for neurokinin B (NKB), a tachykinin peptide primarily found in the arcuate nucleus (ARC) of the hypothalamus iVMS: Induced Vasomotor Symptoms where Hormone Replacement Therapy (HRT) is likely contraindicated Induced vasomotor symptoms (iVMS) are well documented with the use of hormonal cancer therapies and certain surgical procedures Symptoms such as hot flashes can appear immediately and be severe Traditional HRTs are usually contraindicated Acer licensed worldwide rights to osanetant from Sanofi in January 2019 Anticipate submitting IND in Q4 2019 Multiple potential orphan opportunities Little competition in iVMS space Clinical and laboratory safety results are available from 21 completed Phase 1 and 2 studies (325 healthy subjects and 665 patients were treated with osanetant) Oral bioavailability, readily crosses the blood-brain barrier Osanetant Mechanism of Action Disease Overview The Opportunity Product Profile Osanetant: Overview * Am J Psychiatry. 2004 Jun;161(6):975-84.

Acer acquired worldwide rights to osanetant from Sanofi in January 2019 Osanetant (SR142801) was the first selective non-peptide tachykinin NK3 receptor antagonist evaluated as a potential treatment for schizophrenia Clinical and laboratory safety results are available from 21 completed Phase 1 and 2 studies in which 325 healthy subjects and 665 schizophrenic patients were treated with osanetant No major safety concerns identified from these studies after single-dose and repeated-dose administration of up to 400 mg QD for up to 21 days, and 200 mg QD for up to 6 weeks In March 2005, Sanofi-Aventis discontinued the development of osanetant citing ‘lack of efficacy compared with placebo’ in this indication as a major reason for this decision Osanetant History

VMS, typically comprised of hot flashes and night sweats, are associated with decreases in reproductive hormones commonly associated with menopause (e.g. MR-VMS) While VMS associated with menopause can often be treated with hormone replacement therapy (HRT), there are patients who experience VMS who are not in menopause and for whom HRT is likely contraindicated… Osanetant Vasomotor Symptoms (VMS): Overview The Oncologist, Oct 2003, vol.8 no.5 474-487. http://www.everydayhealth.com/menopause/science-behind-the-hot-flash.aspx A diminished amount of hormones, such as estrogen, affects the hypothalamus This confuses the hypothalamus and makes it read “too hot” The brain responds by relaying an alert to cool off The body then tries to cool off by beginning to perspire

Osanetant Induced Vasomotor Symptoms (iVMS) Women with HR+ Breast Cancer (CaB) receiving Tamoxifen 84% of women experienced hot flashes1 80% experienced night sweats 60% experienced severe symptoms Symptoms persisted throughout 5 years of treatment and were mainly attributed to tamoxifen After 4.5 years, 46% of women had discontinued tamoxifen2 Women who are BRCA+ and have prophylactic bilateral salpingo-oophorectomy (PBSO) 67% of women have symptoms of menopause such as hot flashes5 Up to 35% complain of “extremely bothersome” symptoms up to two years after their surgery6 Men with HR+ Prostate Cancer (CaP) receiving Leuprolide 80% of men experience hot flashes3 15-27% of patients consider hot flashes the most distressing side effect 30-40% experienced moderate-to-severe symptoms 20% discontinued or disrupted treatment 1 Moon, Z. et al., JOURNAL OF PSYCHOSOMATIC OBSTETRICS & GYNECOLOGY, 2017 VOL. 38, NO. 3, 226–235 2 Nichols, H, et al., JNCI J Natl Cancer Inst, 2015, 1–8 3 Challapalli, A, et al., Clinical and Translational Radiation Oncology 10 (2018) 29–35 4 Abildgaard, J, et al., JNCI Cancer Spectrum, 2018, Vol. 0, No. 0 5 L. Johnson, et al. American Society for Reproductive Medicine, 2014 Vol 102 No. 3, Supplement, e249 6 Griffiths, E, et al: The Obstetrician & Gynaecologist, 2005: 7:23-27

Osanetant iVMS: The Unmet Need Induced vasomotor symptoms (iVMS) are well documented with the use of hormonal cancer therapies and certain surgical procedures Symptoms such as hot flashes can appear immediately and be severe Traditional HRTs are usually contraindicated Non-adherence to therapy can be associated with side effects which increases the mortality risk or shortens the time to recurrence A non-hormonal treatment for iVMS is needed to help ensure breast or prostate cancer patients can start and stay on critical hormonal cancer therapy and BRCA2 post-PBSO can obtain help with significantly impactful and limiting iVMS

Neurokinin B (NKB) belongs to a group of neuropeptides, called tachykinins or neurokinins, that includes substance-P (SP), neurokinin A (NKA), and two N-terminally extended forms of NKA, neuropeptide g and neuropeptide K The biological effects of tachykinins are mediated through specific receptors denoted NK1, NK2, and NK3 NKB is the preferred endogenous ligand of tachykinin NK3 receptors The tachykinin NK3 receptors are located primarily in the brain, while a few receptors are also present in the peripheral nervous system (intestines, placenta) Osanetant NK3 Receptor (Neurokinin B) HUMAN POA Infundibular Nucleus Dyn NKB Erα PR + - KNDy neurone Kisspeptin neurone POA/Infundibular nucleus KiSS1 GnRH neurone ME Pituitary LH/FSH Gonads Sex Steroids Erα PR (sex steroid receptor) NKB3R Neurokinin B receptor) Kiss 1r/JiSS1R (Kisspeptin receptor) KOR (Koppa opioid receptor)

Neurons in the arcuate nucleus of the hypothalamus that express kisspeptin and neurokinin B (Kiss1ARH neurons) are candidates for mediating hot flushes because they are negatively regulated by sex hormones Transient activation of Kiss1ARH neurons following sex-hormone withdrawal contributes to the occurrence of hot flushes via NkB release in the rostral preoptic area Osanetant VMS: Mechanism of Action Padilla, S. et al. A Neural Circuit Underlying the Generation of Hot Flushes. Cell Reports 2018, 24, 271–277. Hot Flush Optogenetic stimulation Conditional ChR2 viral delivery Stimulation Preoptic Area Thermal regulation (neurokinin B) Arcuate Reproduction (kisspeptin) Kiss1Cre neuron OtherARH neuron

Osanetant NK3R Antagonist Clinical POC in VMS Herman Depypere et al., ENDO2017 Fezolinetant is a NK3R antagonist being developed by Astellas Average Daily Hot Flash Frequency Reported as per FDA Guidance fezolinetant 90mg BID (N=40) placebo (N=40) HF Frequency Baseline Week4 Week 12 0 4 8 12 88% 38% 93% 54%* * : % decrease from the baseline BASELINE WEEK 2 WEEK 4 WEEK 6 WEEK 8 WEEK 10 WEEK 12 FUP WK2 p<0.0001 At Week 4: fezolinetant group: 14/40 patients have ZERO hot flash placebo group 2/40 patients have ZERO hot flash

Osanetant NK3R Antagonist Clinical POC in VMS Prague J., et al. Menopause. 2018 Aug;25(8):862-869. Pavinetant (MLE4901) was a NK3R antagonist that was discontinued by Millendo Hot flash frequency Hot flash severity Hot flash bother Hot flash interference % change from baseline day3 Wk 1 Wk 2 Wk 3 Wk 4 Placebo MLE4901 -100 -80 -60 -40 -20 0 20 FIG.2 Hot flash frequency (A), severity (B), bother (C), and interference (D) outcomes: results are presented as percentage change with 95% CIs from baseline at each time point during the treatment period (i.e. on day 3 of treatment, and then weekly mean total for each week (wk) of the 4-week treatment period for both placebo (white) and MLE4901 (gray). Minimum n = 33; maximum n = 37. *p<0.0001, #P=0.0006, ^P=0.0001, +P=0.0001. Week 4 data adapted from Prague et al, Lancet, 201718.

Acer is partnering with a leading university to design & conduct a clinical trial to evaluate osanetant in various patient populations with iVMS These include patients with medically or surgically iVMS (may include any/all of the following): Women with HR+ Breast Cancer receiving tamoxifen Men with HR+ Prostate Cancer receiving leuprolide Women who are BRCA+ and have had a prophylactic bilateral oophorectomy This initial Phase 1/2 trial would evaluate: PK/PD and Safety, including physiologic PD Identify the optimal dosing strategy to advance into further efficacy studies in minimizing the iVMS symptoms Osanetant Osanetant: Clinical Development Plan

Competitive Landscape Osanetant Program / Company Indication MOA Status VERU-944 (Veru) iVMS in PC on ADT ER agonist Ph 2 Q-122 (Que Oncology) iVMS in BC on Tamoxifen or AIs CRCX4 modulator Ph 2 Fezolinetant (Astellas) VMS – Menopause NK3R antagonist Ph 3 NT-814 (KaNDy Therapeutics) VMS – Menopause NK1/3R antagonist Ph 2 FP-101 (Fervent Pharma) VMS in postmenopausal Undisclosed Non-Hormonal Therapy Ph 2 MT-8554 (Mitsubishi Tanabe) VMS Undisclosed Non-Hormonal Therapy Ph 2 PH80-HF (Pherin Pharma) VMS Undisclosed Ph 2 Donesta (Mithra) VMS Native estrogen Ph 2 AUS-131 (Ausio Pharma) VMS ERβ agonist Ph 2

Acer acquired worldwide rights to osanetant from Sanofi in January 2019 Data from clinical proof of concept studies with other NK3R antagonists suggest rapid and potentially clinically meaningful improvement in vasomotor symptoms Ogeda SA was acquired by Astellas in 2017 for up to €800M Clinical and laboratory safety results are available from 21 completed Phase 1 and 2 studies in which 325 healthy subjects and 665 schizophrenic patients were treated with osanetant Osanetant would be a New Chemical Entity (NCE) in the US, and as such would be eligible for five years’ market exclusivity from potential FDA approval Additional exclusivity (e.g. Orphan Drug Designation) will depend upon indication(s) and development pathway chosen Anticipate IND submission in Q4 2019 Initiation of Phase 1/2 trial anticipated mid-2020, subject to additional capital Osanetant Market Opportunity and IP

Cash: $23.5M as of June 30, 2019 Expected to have sufficient capital through end of 2020 Capitalization as of June 30, 2019: 10.1M shares of common stock outstanding 11.1M shares of common stock fully diluted $87M invested through August 2018 ACER Financial Overview

Summary ACER Acer’s pipeline includes three clinical-stage product candidates: EDSIVO™ (celiprolol) for the treatment of vascular Ehlers-Danlos syndrome (vEDS) in patients with a confirmed type III collagen (COL3A1) mutation ACER-001 (a fully taste-masked, immediate release formulation of sodium phenylbutyrate) for the treatment of various inborn errors of metabolism, including urea cycle disorders (UCDs) and Maple Syrup Urine Disease (MSUD) Osanetant for the treatment of induced Vasomotor Symptoms (iVMS) where Hormone Replacement Therapy (HRT) is likely contraindicated Acer’s product candidates are believed to present a comparatively de-risked profile, having one or more of: Favorable safety profile; Clinical proof-of-concept data; Mechanistic differentiation Accelerated paths for development through specific FDA-established programs Multiple anticipated key regulatory milestones: EDSIVO™ Type A mtg w/FDA:Q3 2019 ACER-001 (UCD) pivotal bridging & taste assessment trials initiation:Q4 2019 Osanetant IND submission:Q4 2019 ACER-001 (UCD) NDA submission*:Mid-2020 Osanetant Phase 1/2 PK/PD/safety trial initiation**:Mid-2020 Expected to have sufficient capital through end of 2020 * Assuming successful outcomes in bridging trials and NDA submission with 6 months stability data ** Subject to additional capital