– Announced topline results from Phase 2 Trial of ABP-450 (prabotulinumtoxinA) for the preventive treatment of episodic migraine that support advancing the program into a pivotal Phase 3 study –
– Ongoing Phase 2 trial for the preventive treatment of chronic migraine has enrolled over 430 subjects; anticipate completing enrollment in Q4 2023 and announcing topline data in 2H 2024 –
– Successfully completed business combination transaction and associated equity financings –
“Over the past several months, we have successfully executed our strategy with the announcement of clinical data that support the advancement of our ABP-450 programs and position the Company to finance our ongoing and planned clinical trials,” commented
Recent Clinical and Corporate Highlights
- Topline data from Episodic Migraine Phase 2 Study:
- Announced topline results from the Phase 2 clinical trial of ABP-450 (prabotulinumtoxinA) for the preventive treatment of episodic migraine, which showed ABP-450 had a treatment effect with mean reductions in MMD of 4.8 days at the 150U dose and 5.0 days at the 195U dose, compared to only 4.2 days in placebo at weeks 21-24, but did not meet statistical significance. ABP-450 did achieve statistical significance and clinically meaningful separation from placebo across most of the study’s key prespecified secondary endpoints. Also, ABP-450 demonstrated a favorable safety profile for patients with episodic migraine.
- The Company believes the totality of the Phase 2 data provides evidence of a dose response favoring the higher 195U dose and lends support to progress ABP-450 into Phase 3.
- Presentation of Full Data from Cervical Dystonia (CD) Phase 2 Study - Presented positive full results from the Phase 2 clinical study of ABP-450 for the treatment of CD at the International Parkinson and Movement Disorders Society Congress® (IP-MDS). These data, previously released by the Company in
September 2022 , include showing relatively sustained benefits across all doses of ABP-450 in Toronto Western Spasmodic Torticollis rating scale (TWSTRS) total score and safety data that further support the Company’s strategy to pursue ABP-450 as an approved therapy for CD. - New
U.S. Patent - Received a notice of allowance from the United States Patent and Trademark Office (“USPTO”) forU.S. Patent Application No. 17/006,685, titled “Neurotoxin Compositions for Use in Treating Headache” (the “Application”), which will provide protection in theU.S. for the claimed methods of use of ABP-450 (prabotulinumtoxinA) injection into 2041. - Common Stock (AEON) and Warrants (AEON WS) Listed on NYSE American - Completed the Company’s listing of its common stock and warrants on NYSE American following the closing of the business combination with
Priveterra Acquisition Corp. , a special purpose acquisition company (the “Merger”). - Post-Merger Funding - Closed the Company’s funding arrangements, which included approximately
$50 million of committed financing from existing and new AEON investors, as well as the cash remaining in Priveterra’s trust account after redemptions. - Cash, Cash Equivalents and Investments – The Company reported cash, cash equivalents and investments were approximately
$16.2 million as ofSeptember 30, 2023 . The Company believes its cash, cash equivalents and investments will be sufficient to fund its planned clinical studies, as well as support corporate operations intomid-December 2023 .
Key Upcoming Milestones
- Episodic Migraine Program Next Steps - The Company plans to request an end-of-phase 2 meeting with the
U.S. Food and Drug Administration (FDA) to discuss the protocol and study design for Phase 3, and the meeting is expected to take place in the first half of 2024. The Company is evaluating multiple parameters for the Phase 3 trial that are expected to increase the statistical power and reduce the observed higher placebo responses reported in the Phase 2 study. - Ongoing Chronic Migraine Phase 2 Study - On track to complete enrollment in the ongoing Phase 2 study of ABP-450 as a preventive treatment for chronic migraine in the fourth quarter of 2023 and announce the topline data in the second half of 2024.
About Migraine
Migraine is a complex neurological disease characterized by recurrent episodes of headaches that affects approximately 40 million people in
About ABP-450 (prabotulinumtoxinA) Injection
ABP-450 contains a 900 kDa botulinum toxin type-A complex produced by the bacterium Clostridium botulinum. The active part of the botulinum toxin is the 150 kDa component, and the remaining 750 kDa of the complex is made up of accessory proteins that the Company believes help with the function of the active portion of the botulinum toxin. When injected at therapeutic levels, ABP-450 blocks peripheral acetylcholine release at presynaptic cholinergic nerve terminals by cleaving SNAP-25, a protein integral to the successful docking and release of acetylcholine from vesicles situated within the nerve endings leading to denervation and relaxation of the muscle.
About AEON Biopharma
AEON is a clinical stage biopharmaceutical company focused on developing its proprietary botulinum toxin complex, ABP-450 (prabotulinumtoxinA) injection, or ABP-450, for debilitating medical conditions, with an initial focus on the neurosciences market. AEON recently completed a Phase 2 study of ABP-450 for the treatment of cervical dystonia and has an ongoing Phase 2 study of ABP-450 for the preventive treatment of chronic migraine. ABP-450 is the same botulinum toxin complex that is currently approved and marketed for cosmetic indications by Evolus under the name Jeuveau. ABP-450 is manufactured by Daewoong in compliance with current Good Manufacturing Practice, or cGMP, in a facility that has been approved by the
Forward-Looking Statements
Certain statements in this press release may be considered forward-looking statements. Forward-looking statements generally relate to future events or AEON’s future financial or operating performance. For example, statements regarding continued listing on NYSE American, the anticipated timing of clinical results, the impact of current financing arrangements, the competitive environment in which AEON operates, AEON’s expected capital resources and liquidity needs and the expected future operating and financial performance and market opportunities of AEON are forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as "pro forma", "may", "should", "could", "might", "plan", "possible", "project", "strive", "budget", "forecast", "expect", "intend", "will", "estimate", "anticipate", "believe", "predict", "potential" or "continue", or the negatives of these terms or variations of them or similar terminology. Such forward-looking statements are subject to risks, uncertainties, and other factors which could cause actual results to differ materially from those expressed or implied by such forward-looking statements.
These forward-looking statements are based upon estimates and assumptions that, while considered reasonable by AEON and its management, are inherently uncertain. Factors that may cause actual results to differ materially from current expectations include, but are not limited to: (i) the outcome of any legal proceedings that may be instituted against AEON or others; (ii) AEON’s future capital requirements, including with respect to potential obligations pursuant to the forward purchase agreements; (iii) AEON’s ability to raise financing in the future; (iv) AEON’s ability to continue to meet continued stock exchange listing standards; (v) costs related to being a public company; (vi) changes in applicable laws or regulations; (vii) the possibility that AEON may be adversely affected by other economic, business, regulatory, and/or competitive factors; (viii) AEON’s estimates of expenses and profitability; (ix) the evolution of the markets in which AEON competes; (x) the ability of AEON to implement its strategic initiatives, including the continued development of ABP-450; (xi) the ability of AEON to defend its intellectual property; (xii) the ability of AEON to satisfy regulatory requirements; (xiii) the impact of adverse geopolitical and macroeconomic developments, such as the COVID-19 pandemic, the Israel-Hamas conflict, the
Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. AEON does not undertake any duty to update these forward-looking statements.
Contacts
Investor Contact:
+1 212 915 2577
cdavis@lifesciadvisors.com
Source: AEON Biopharma
AEON CONDENSED CONSOLIDATED BALANCE SHEETS (in thousands, except share data and par value amounts) | |||||||||
Successor | Predecessor | ||||||||
2023 | 2022 | ||||||||
(Unaudited) | |||||||||
ASSETS | |||||||||
Current assets: | |||||||||
Cash | $ | 16,177 | $ | 9,746 | |||||
Prepaid expenses and other current assets | 734 | 92 | |||||||
Total current assets | 16,911 | 9,838 | |||||||
Property and equipment, net | 356 | 431 | |||||||
Operating lease right-of-use asset | 323 | 475 | |||||||
Other assets | 29 | 34 | |||||||
Total assets | $ | 17,619 | $ | 10,778 | |||||
LIABILITIES, CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS' DEFICIT | |||||||||
Current liabilities: | |||||||||
Accounts payable | $ | 4,013 | $ | 7,805 | |||||
Accrued clinical trials expenses | 5,641 | 2,051 | |||||||
Accrued compensation | 1,020 | 1,112 | |||||||
Excise tax payable | 569 | — | |||||||
Other accrued expenses | 2,934 | 740 | |||||||
Current portion of convertible notes at fair value, including related party amount of | — | 70,866 | |||||||
Total current liabilities | 14,177 | 82,574 | |||||||
Convertible notes at fair value, including related party amount of | — | 60,426 | |||||||
Operating lease liability | 52 | 242 | |||||||
Warrant liability | 2,172 | — | |||||||
Contingent consideration liability | 74,505 | — | |||||||
Embedded forward purchase agreements and derivative liabilities | 48,453 | — | |||||||
Total liabilities | 139,359 | 143,242 | |||||||
Commitments and contingencies | |||||||||
Convertible preferred stock issuable in series, | — | 137,949 | |||||||
Stockholders’ Deficit: | |||||||||
Class A common stock, | 4 | 14 | |||||||
Additional paid-in capital | 362,114 | 187,348 | |||||||
Subscription receivables | (60,710 | ) | — | ||||||
Accumulated deficit | (423,148 | ) | (474,839 | ) | |||||
— | (23 | ) | |||||||
(121,740 | ) | (287,500 | ) | ||||||
Non-controlling interest | — | 17,087 | |||||||
Total stockholders' deficit | (121,740 | ) | (270,413 | ) | |||||
Total liabilities, convertible preferred stock and stockholders' deficit | $ | 17,619 | $ | 10,778 |
AEON CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (in thousands, except share and per share data) (Unaudited) | ||||||||||||||||||||||||||
Three Months Ended | Nine Months Ended | |||||||||||||||||||||||||
2023 | 2022 | 2023 | 2022 | |||||||||||||||||||||||
Predecessor | Successor | Predecessor | Predecessor | Successor | Predecessor | |||||||||||||||||||||
Operating expenses: | ||||||||||||||||||||||||||
Selling, general and administrative | $ | 1,055 | $ | 5,460 | $ | 2,436 | $ | 9,841 | $ | 5,460 | $ | 8,171 | ||||||||||||||
Research and development | 1,573 | 6,383 | 7,477 | 19,803 | 6,383 | 25,225 | ||||||||||||||||||||
Change in fair value of contingent consideration | — | (69,715 | ) | — | — | (69,715 | ) | — | ||||||||||||||||||
Total operating costs and expenses | 2,628 | (57,872 | ) | 9,913 | 29,644 | (57,872 | ) | 33,396 | ||||||||||||||||||
(Loss) income from operations | (2,628 | ) | 57,872 | (9,913 | ) | (29,644 | ) | 57,872 | (33,396 | ) | ||||||||||||||||
Other (loss) income: | ||||||||||||||||||||||||||
Change in fair value of convertible notes | 2,582 | — | (666 | ) | (3,528 | ) | — | 15,261 | ||||||||||||||||||
Change in fair value of warrants | — | 1,593 | — | — | 1,593 | — | ||||||||||||||||||||
Change in fair value of embedded forward purchase agreements and derivative liabilities | (4,959 | ) | (15,776 | ) | — | (4,959 | ) | (15,776 | ) | — | ||||||||||||||||
Other income, net | 5 | 186 | 141 | 114 | 186 | 142 | ||||||||||||||||||||
Total other (loss) income, net | (2,372 | ) | (13,997 | ) | (525 | ) | (8,373 | ) | (13,997 | ) | 15,403 | |||||||||||||||
(Loss) income before taxes | (5,000 | ) | 43,875 | (10,438 | ) | (38,017 | ) | 43,875 | (17,993 | ) | ||||||||||||||||
Income taxes | — | — | — | — | — | — | ||||||||||||||||||||
(Loss) Income and comprehensive (loss) income | $ | (5,000 | ) | $ | 43,875 | $ | (10,438 | ) | $ | (38,017 | ) | $ | 43,875 | $ | (17,993 | ) | ||||||||||
Basic and diluted net (loss) income per share | $ | (0.04 | ) | $ | 1.19 | $ | (0.08 | ) | $ | (0.28 | ) | $ | 1.19 | $ | (0.13 | ) | ||||||||||
Weighted average shares of common stock outstanding used to compute basic and diluted net (loss) income per share | 138,848,177 | 37,159,600 | 138,848,177 | 138,848,177 | 37,159,600 | 138,848,177 |
The accompanying condensed consolidated financial statements have been prepared in accordance with generally accepted accounting principles in
On
Unless the context otherwise requires, the “Company,” for periods prior to the close of the Merger, refers to Old AEON, currently
Source: AEON Biopharma
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