AEON Biopharma Files S-1/A for Share Registration

Ticker: AEON · Form: S-1/A · Filed: May 31, 2024 · CIK: 1837607

Sentiment: neutral

Topics: registration-statement, biotech, financing

TL;DR

AEON Biopharma registering 6.97M shares, cash up to $138.8M. Big move for biotech investors.

AI Summary

AEON Biopharma, Inc. filed an S-1/A on May 31, 2024, to register 6,971,500 shares of common stock. The company, formerly Priveterra Acquisition Corp., is focused on developing treatments for diseases, with a primary candidate, ABP-101, for glioblastoma. The filing indicates a significant increase in cash and cash equivalents from $37.16 million to $138.85 million.

Why It Matters

This filing is crucial for investors as it details the registration of a substantial number of shares, potentially impacting the stock's liquidity and valuation. It also provides updated financial figures for AEON Biopharma.

Risk Assessment

Risk Level: medium — The company is in the pharmaceutical development stage, which inherently carries high risks related to clinical trials, regulatory approval, and market adoption.

Key Numbers

Key Players & Entities

FAQ

What is the primary purpose of this S-1/A filing for AEON Biopharma, Inc.?

The primary purpose is to register 6,971,500 shares of common stock for potential sale or issuance.

What was AEON Biopharma, Inc.'s former name?

AEON Biopharma, Inc. was formerly known as Priveterra Acquisition Corp.

What is the reported amount of cash and cash equivalents for AEON Biopharma as of the filing date?

As of the filing date, AEON Biopharma reported $138,848,177 (approximately $138.85 million) in cash and cash equivalents.

When was this S-1/A filing submitted?

This S-1/A filing was submitted on May 31, 2024.

What is AEON Biopharma's business focus?

AEON Biopharma is focused on developing treatments for diseases, with a specific mention of ABP-101 for glioblastoma.

Filing Stats: 4,491 words · 18 min read · ~15 pages · Grade level 17.2 · Accepted 2024-05-31 16:03:33

Key Financial Figures

Filing Documents

USE OF PROCEEDS

USE OF PROCEEDS 56 DIVIDEND POLICY 57

MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS 58

BUSINESS

BUSINESS 79 MANAGEMENT 108 EXECUTIVE AND DIRECTOR COMPENSATION 114 CERTAIN RELATIONSHIPS AND RELATED PARTY TRANSACTIONS 130 PRINCIPAL STOCKHOLDERS 139 REGISTERED HOLDERS 141 DESCRIPTION OF OUR SECURITIES 151 PLAN OF DISTRIBUTION 162 LEGAL MATTERS 165 EXPERTS 166 WHERE YOU CAN FIND MORE INFORMATION 167 INDEX TO FINANCIAL STATEMENTS F-1 i Table of Contents ABOUT THIS PROSPECTUS This prospectus is part of a registration statement that we filed with the United States Securities and Exchange Commission, or the SEC, using a "shelf" registration process. We will not receive any proceeds from the sale by the Registered Holders of the securities offered by them described in this prospectus. This prospectus also relates to the issuance by us of the shares of Common Stock issuable upon the exercise of the Warrants. We will not receive any proceeds from the sale of shares of Common Stock underlying the Warrants pursuant to this prospectus, except with respect to amounts received by us upon the exercise of the Warrants for cash. We may also file a prospectus supplement or post-effective amendment to the registration statement of which this prospectus forms a part that may contain material information relating to these offerings. The prospectus supplement or post-effective amendment may also add, update or change information contained in this prospectus with respect to that offering. If there is any inconsistency between the information in this prospectus and the applicable prospectus supplement or post-effective amendment, you should rely on the prospectus supplement or post-effective amendment, as applicable. Before purchasing any securities, you should carefully read this prospectus, any post-effective amendment, and any applicable prospectus supplement, together with the additional information described under the heading " Where You Can Find More Information ." Neither we nor the Registered Holders have authorized anyone to provide y

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