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8-K

BioXcel Therapeutics, Inc. (BTAI)

8-K 2022-09-12 For: 2022-09-12
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Added on April 11, 2026


UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d) ofthe

Securities Exchange Act of 1934

Date of Report (Date of earliest event reported) September 12, 2022


BioXcel Therapeutics, Inc.

(Exact name of registrant as specified in its charter)

Delaware 001-38410 82-1386754
(State<br> or other jurisdiction of<br><br> incorporation) (Commission<br> File Number) (IRS<br> Employer<br><br> Identification No.)

555 Long Wharf Drive

New Haven, CT 06511

(Address of principal executive offices, including Zip Code)

(475) 238-6837

(Registrant’s telephone number, including area code)

N/A

(Former name or former address, if changed since last report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

¨ Written communications pursuant to Rule 425 under the Securities<br>Act (17 CFR 230.425)
¨ Soliciting material pursuant to Rule 14a-12 under the Exchange<br>Act (17 CFR 240.14a-12)
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¨ Pre-commencement communications pursuant to Rule 14d-2(b) under<br>the Exchange Act (17 CFR 240.14d-2(b))
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¨ Pre-commencement communications pursuant to Rule 13e-4(c) under<br>the Exchange Act (17 CFR 240.13e-4(c))
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Securities registered pursuant to Section 12(b) of the Act:

Title of each class Trading Symbol(s) Name of each exchange on which registered
Common Stock, par value $0.001 BTAI The Nasdaq Capital Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company   x

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.   x

Item 8.01 Other Events.

As previously announced, Dr. Vimal Mehta, Founder and Chief Executive Officer of BioXcel Therapeutics, Inc. (the “Company”), will be participating in a fireside chat at the H.C. Wainwright 24th Annual Global Investment Conference (the “Conference”) on Monday, September 12, 2022 at 10:30 a.m. Eastern Time. Dr. Mehta will discuss updates for the Company’s neuroscience and immuno-oncology programs as well as its artificial intelligence platform used to augment and accelerate the drug candidate discovery and development process. He will also discuss the Company’s commercial launch strategy for IGALMI™ (dexmedetomidine) sublingual film as well as the Company’s financial condition. The presentation materials that will be used at the Conference as well as a live webcast will be available under “News/Events” within the Investors & Media section of the Company’s website at www.bioxceltherapeutics.com. A replay of the webcast will be available on the Company’s website following the event. Select slides from the presentation materials are filed as Exhibit 99.1 hereto and incorporated by reference herein.

Forward-Looking Statements

Statements in this Form 8-K regarding management’s future expectations, beliefs, intentions, goals, strategies, plans or prospects are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited, to statements regarding the Company’s expected timing of, and data results from, trials and clinical studies involving its product candidates; planned discussions with regulators; its commercial plan and strategy for IGALMI™ and strategic options for OnkosXcel; and its future financial and operational results. Forward-looking statements may be identified by words such as “anticipates,” “believe,” “continue,” “expect,” “intend,” “may,” “plan to,” “potential,” “projects,” “will,” and other similar words or expressions, or the negative of these words or similar words or expressions. In addition, any statements or information that refer to expectations, beliefs, plans, projections, objectives, performance, or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking. All forward-looking statements are based upon the Company’s current expectations and various assumptions. The Company believes there is a reasonable basis for its expectations and beliefs, but they areinherently uncertain. The Company may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described or implied by such forward-looking statements as a result of various important factors, including, without limitation: its limited operating history; its incurrence of significant losses; its need for substantial additional funding and ability to raise capital when needed; its limited experience in drug discovery and drug development; its dependence on the success and commercialization of IGALMI™, BXCL501, BXCL502 and BXCL701 and other product candidates; the Company has no experience in marketing and selling drug products; IGALMI™ or the Company’s product candidates may not be accepted by physicians or the medical community in general; the failure of preliminary data from its clinical studies to predict final study results; failure of its early clinical studies or preclinical studies to predict future clinical studies;its ability to receive regulatory approval for its product candidates; its ability to enroll patients in its clinical trials; undesirable side effects caused by the Company’s product candidates; its novel approach to the discovery and development of product candidates based on EvolverAI; its exposure to patent infringement lawsuits; its ability to comply with the extensive regulations applicable to it; impacts from the COVID-19 pandemic; its ability to commercialize its product candidates; and the other important factors discussed under the caption "Risk Factors" in its Quarterly Report on Form 10-Q for the quarterly period ended June 30, 2022, as such factors may be updated from time to time in its other filings with the SEC, which are accessible on the SEC's website at www.sec.gov and the Investors section of our website at www.bioxceltherapeutics.com. All forward-looking statements speak only as of the date of this Form 8-K and, except as required by applicable law, the Company has no obligation to update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

Item****9.01. Financial Statements and Exhibits

(d)       Exhibits


Exhibit No. Description
99.1 Slides from Investor Fireside Chat, dated September 12, 2022.
104 Cover Page Interactive Data File (embedded within the Inline XBRL document)

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Date: September 12, 2022 BIOXCEL THERAPEUTICS, INC.
/s/ Richard Steinhart
Richard Steinhart
Chief Financial Officer

Exhibit 99.1

®<br>BioXcel Therapeutics 555 Long Wharf Drive, 12th Floor New Haven, CT 06511 www.bioxceltherapeutics.com<br>September 2022<br>AI-Driven Drug Development<br>in Neuroscience and<br>Immuno-oncology<br>NASDAQ: BTAI
This presentation includes "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995.Forward-looking statements in this<br>presentation include but are not limited to: statements regarding BioXcel Therapeutics’ expected timing of, and data results from, trials and clinical studies involving its product<br>candidates; planned discussions with regulators; its commercial plan and strategy for IGALMI™ and strategic options for OnkosXcel; potential market size and opportunity for<br>products and product candidates, and its future financial and operational results. When used herein, words including "anticipate," "being," "will," "plan," "may," "continue," and<br>similar expressions are intended to identify forward-looking statements. In addition, any statements or information that refer to expectations, beliefs, plans, projections,<br>objectives, performance, or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking. All forward-looking statements<br>are based upon BioXcel Therapeutics’ current expectations and various assumptions. BioXcel Therapeutics believes there is a reasonable basis for its expectations and<br>beliefs, but they are inherently uncertain.<br>BioXcel Therapeutics may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described or implied by such<br>forward-looking statements as a result of various important factors, including, without limitation: its limited operating history; its incurrence of significant losses; its need for<br>substantial additional funding and ability to raise capital when needed; its limited experience in drug discovery and drug development; its dependence on the success and<br>commercialization of IGALMI™, BXCL501, BXCL502 and BXCL701 and other product candidates; the Company has no experience in marketing and selling drug products;<br>IGALMI™ or the Company’s product candidates may not be accepted by physicians or the medical community in general; the failure of preliminary data from its clinical studies<br>to predict final study results; failure of its early clinical studies or preclinical studies to predict future clinical studies; its ability to receive regulatory approval for its product<br>candidates; its ability to enroll patients in its clinical trials; undesirable side effects caused by the Company’s product candidates; its novel approach to the discovery and<br>development of product candidates based on EvolverAI; its exposure to patent infringement lawsuits; its ability to comply with the extensive regulations applicable to it; impacts<br>from the COVID-19 pandemic; its ability to commercialize its product candidates; and the other important factors discussed under the caption "Risk Factors" in its Quarterly<br>Report on Form 10-Q for the quarterly period ended June 30, 2022, as such factors may be updated from time to time in its other filings with the SEC, which are accessible on<br>the SEC's website at www.sec.gov and the Investors section of our website at www.bioxceltherapeutics.com.<br>These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this presentation. Any such<br>forward-looking statements represent management's estimates as of the date of this presentation. While BioXcel Therapeutics may elect to update such forward-looking<br>statements at some point in the future, except as required by law, it disclaims any obligation to do so, even if subsequent events cause our views to change. These forward-<br>looking statements should not be relied upon as representing BioXcel Therapeutics’ views as of any date subsequent to the date of this presentation.<br>Forward-Looking Statements<br>2
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Compound Indication/Proposed Indication Preclinical Phase 1 Phase 2 Phase 3 Registration Marketed<br>Neuroscience<br>BXCL501<br>At-home acute treatment of agitation associated<br>with schizophrenia or bipolar I or II disorder<br>in adults<br>Acute treatment of agitation associated with<br>Alzheimer’s disease*<br>Adjunctive treatment in major depressive disorder<br>BXCL502 Chronic agitation in Alzheimer’s disease<br>Wearable<br>Device<br>(+BXCL501)**<br>Pre & post-agitation in dementia<br>Immuno-oncology<br>BXCL701 Metastatic castration-resistant prostate cancer<br>(small cell neuroendocrine and adenocarcinoma)<br>Potential Market-Changing Product & Current Pipeline<br>Pipeline as of Sept. 12, 2022<br>The safety and efficacy of investigational agents and/or investigational uses of approved products have not been established<br>*Includes intermittent chronic agitation<br>**Regulatory path to be determined; device + drug combination to be evaluated after further evaluation of predictive algorithm<br>Approved April 5, 2022<br>(Combination with KEYTRUDA®)<br>Phase 0<br>device testing<br>Approved April 5, 2022 Acute treatment of agitation associated with schizophrenia<br>or bipolar I or II disorder in adults<br>5<br>SERENITY III<br>TRANQUILITY II & III
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Near-Term Catalysts & Key Events<br>NEUROSCIENCE: BXCL501 Timeframe<br>IGALMI™ U.S. Commercial Launch July 2022<br>Alzheimer’s Disease: TRANQUILITY III<br> • Expected study initiation 2H 2022<br>Bipolar Disorders or Schizophrenia (at-home use):<br>SERENITY III<br> • Expected study initiation<br>2H 2022<br>Alzheimer’s Disease: TRANQUILITY II<br> • Top-line data readout 1H 2023<br>Major Depressive Disorder (MDD)<br> • Top-line results from Phase 1 dose-selection trial in healthy<br>volunteers<br>1H 2023<br>IMMUNO-ONCOLOGY: BXCL701<br>Aggressive Variant of Metastatic Castration-Resistant<br>Prostate Cancer<br> • Expected enrollment completion of 28-patient SCNC cohort<br>2H 2022<br>6<br>Anticipated near-term catalysts as of Sept. 12, 2022
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• Optimize R&D economics<br> • Shorten development timelines<br> • Achieve higher probability of<br>success<br>* all 3 driven by comprehensive AI plan<br> • Proprietary EvolverAI™<br>technology platform<br> • BXCL501 – IND acceptance to<br>IGALMI™ approval in 3.5 yrs.<br>- 3 upcoming Phase 3 trials<br> • BXCL701 – Human POC<br>established in SCNC<br>- Leader in DPP 8/9 biology<br>(new checkpoint)<br> • ~39 million* annual episodes<br>of agitation associated with<br>schizophrenia & bipolar<br>disorders in U.S.1,2,3,4<br> • ~100 million annual episodes<br>of agitation associated with<br>Alzheimer’s disease in U.S.5<br> • 300+ million antidepressant<br>prescriptions filled annually6<br> • BXCL501: Alzheimer’s-related<br>agitation -<br>TRANQUILITY II & III -<br>Pivotal program<br> • BXCL501: Bipolar &<br>Schizophrenia-related<br>agitation (at-home setting)<br>- SERENITY III pivotal trial<br> • BCXL701: SCNC clinical POC<br> – 800-patient safety database<br> • Cash runway into 2025**<br> • Well-funded to drive catalysts & long-term growth<br>Unprecedented<br>Value Creation*<br>Clinically Validated<br>AI Platform<br>Transformative Approach With Technology, Business Model, and Medicines<br>Strong Value Proposition and Long-Term Growth Potential<br>7<br>Large Market<br>Opportunity<br>Strong Financial Position<br>Advanced Pipeline<br>*Includes 16 million institutional episodes, 9 million at-home Rx episodes, as well as 14 million self-managed episodes<br>**Assumes full execution of strategic financing agreements announced on April 19, 2022, including funding of remaining tranches subject to regulatory and financial milestones and certain other conditions .<br>1. Wu, 2006, NAMI 2. NIMH- Prevalence of bipolar disorder in adults. November 2017. Accessed June 24, 2021. https://www.hcp.med.harvard.edu/ncs/ftpdir/NCS-R_12-month_Prevalence_Estimates.pdf 3. Data on File<br>4. inVibe Patient Agitation Market Research, July 2022 (n=57) 5. Estimate based on company market research 6 NIH/WHO, SAMHSA, NIMH Pratt et al, 2017
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Significant Market Opportunity:<br>Agitation in Bipolar Disorders & Schizophrenia<br>15<br>1. Wu, 2006, NAMI 2. NIMH- Prevalence of bipolar disorder in adults. November 2017. Accessed June 24, 2021. https://www.hcp.med.harvard.edu/ncs/ftpdir/NCS-R_12-<br>month_Prevalence_Estimates.pdf 3. Data on File 4. inVibe Patient Agitation Market Research, July 2022 (n=57) 5. 39M episodes @ $105/episode<br>16M<br>Institutional<br>Episodes1-3<br>9M<br>At-Home Rx<br>Episodes1-3<br>14M<br>Self-<br>Managed<br>Episodes1-4<br>$4B<br>Potential<br>Market<br>Opportunity5<br>SERENITY III Pivotal Trial<br>Institutional Episodes<br>23M Episodes
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Significant Market Opportunity:<br>Agitation in Bipolar Disorders & Schizophrenia<br>23<br>1. Wu, 2006, NAMI 2. NIMH- Prevalence of bipolar disorder in adults. November 2017. Accessed June 24, 2021. https://www.hcp.med.harvard.edu/ncs/ftpdir/NCS-R_12-<br>month_Prevalence_Estimates.pdf 3. Data on File 4. inVibe Patient Agitation Market Research, July 2022 (n=57) 5. 39M episodes @ $105/episode<br>16M<br>Institutional<br>Episodes1-3<br>9M<br>At-Home Rx<br>Episodes1-3<br>14M<br>Self-<br>Managed<br>Episodes1-4<br>$4B<br>Potential<br>Market<br>Opportunity5<br>SERENITY III Pivotal Trial<br>At-Home & Self-Managed Episodes<br>23M Episodes
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