07/24/2026 | Press release | Distributed by Public on 07/24/2026 15:20
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Delaware
(State or other jurisdiction of
incorporation or organization)
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84-1850815
(I.R.S. Employer
Identification Number)
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Large accelerated filer
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☒
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Accelerated filer
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☐
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Non-accelerated filer
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☐
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Smaller reporting company
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☐
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Emerging growth company
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☐
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ABOUT THIS PROSPECTUS
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1
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ABOUT THE COMPANY
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2
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RISK FACTORS
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3
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CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS
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4
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USE OF PROCEEDS
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6
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SELLING STOCKHOLDERS
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7
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PLAN OF DISTRIBUTION
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9
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LEGAL MATTERS
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11
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EXPERTS
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11
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WHERE YOU CAN FIND MORE INFORMATION
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11
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INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
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12
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the continued commercial success of AttrubyTM (acoramidis), including our expectations regarding the size and growth potential of the commercial markets for Attruby;
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the success, cost and timing of our clinical development of our late-stage product candidates, including low-dose infigratinib for achondroplasia, encaleret for ADH1, and BBP-418 for limb-girdle muscular dystrophy type 2I/R9, or LGMD2I/R9;
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our ability to continue planned preclinical and clinical development of our respective development programs, and the timing, cost and success of any such continued preclinical and clinical development and planned regulatory submissions;
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our ability to initiate, recruit and enroll patients in and conduct our clinical trials at the pace that we project;
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the expected timing of our regulatory submissions, and our anticipated interaction with and feedback from the U.S. Food and Drug Administration (the "FDA") and similar regulatory authorities;
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our plans to implement certain development strategies, including our ability to attract and retain potential collaborators with development, regulatory and commercialization expertise;
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our ability to obtain and maintain regulatory approval of our product candidates in any of the indications for which we are developing or we plan to develop, and any related restrictions, limitations or warnings in the label of any of our product candidates, if approved;
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our ability to successfully commercialize our current product candidates, if approved, and any other product candidates we may identify and pursue, if approved, including our ability to successfully build a specialty sales force and commercial infrastructure to market our current product candidates and any other product candidates we may identify and pursue;
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our ability to compete with companies currently marketing approved treatments or engaged in the development of treatments that may become available for any of the indications that our product candidates are designed to target;
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our reliance on third parties to conduct our clinical trials and to manufacture drug substance and drug product for our commercial product and certain of our product candidates for use in our clinical trials;
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our ability to contract with and the performance of our and our collaborators' third-party suppliers and manufacturers;
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the pricing and reimbursement of our product candidates, if approved;
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the size and growth potential of the markets for our current product candidates or other product candidates we may identify and pursue, and our ability to serve and gain acceptance by those markets;
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our ability to identify and advance through clinical development any additional product candidates;
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the impacts of public health crises or macroeconomic factors that could impact our business, such as the effects of the ongoing conflicts in the Ukraine or in the Middle East on the global economy; supply chain and inflationary pressures, or significant political, trade or regulatory developments in the jurisdictions in which we may sell our products or conduct our operations;
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our ability to retain and recruit key personnel;
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the success of competing therapies that are or may become available;
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our ability to obtain and maintain adequate intellectual property rights for our product candidates and our ability to operate our business without infringing on the intellectual property rights of others;
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our expectations regarding government and third-party payor coverage and reimbursement;
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our estimates of our expenses, ongoing losses, capital requirements and our use of cash resources, and our needs for or ability to pay for debt interests and obtain additional financing to complete the clinical trials of any of our product candidates;
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the impact of laws and regulations in the United States and foreign countries;
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our financial performance, including our anticipated funding to support the potential launch of three additional medicines globally;
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adverse developments affecting the financial services industry, such as actual events or concerns involving liquidity, defaults, or non-performance by financial institutions or transactional counterparties; and
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developments and projections relating to our competitors or our industry.
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Shares Beneficially
Owned Before this
Offering
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Number of
Shares
Offered
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Shares
Beneficially
Owned
After this
Offering(4)
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Name of Selling Stockholder
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Shares
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%
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Shares
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%
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KKR Genetic Disorder L.P. and its affiliates(1)
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14,232,739
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7.3%
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14,232,739
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0
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*
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Chinotto Investments, LLC(2)
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5,805,936
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2.9%
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5,805,936
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0
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*
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Aisling Capital IV, LP(3)
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4,589,611
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2.3%
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6,068,125
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0
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*
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*
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Less than 1%.
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(1)
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Consists of (i) 13,260,971 shares of common stock directly held by KKR Genetic Disorder L.P. and (ii) 971,768 shares of common stock issuable upon conversion of 133,900 shares of the Preferred Stock, based on the initial conversion price of $137.79 per share and without giving effect to any shares issuable in respect of accrued and accumulated dividends shares of common stock, directly held by HCRx Investments HoldCo, L.P.
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KKR Genetic Disorder GP LLC, as the general partner of KKR Genetic Disorder L.P., KKR Group Partnership L.P., as the sole member of KKR Genetic Disorder GP LLC, KKR Group Holdings Corp., as the general partner of KKR Group Partnership L.P., KKR Group Co. Inc., as the sole shareholder of KKR Group Holdings Corp., KKR & Co. Inc., as the sole shareholder of KKR Group Co. Inc., KKR Management LLP, as the Series I preferred stockholder of KKR & Co. Inc., and Messrs. Henry R. Kravis and George R. Roberts, as the founding partners of KKR Management LLP, may be deemed to be the beneficial owners having shared voting and investment power with respect to the securities reported herein as being held directly by KKR Genetic Disorder L.P.
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HCRx Master GP, LLC , as the general partner of HCRx Investments HoldCo, L.P., Healthcare Royalty Management, LLC as the investment manager of HCRx Investments HoldCo, L.P., KKR Harbor Holdings L.P., as a member of Healthcare Royalty Management, LLC, KKR Harbor Holdings GP LLC, as the general partner of KKR Harbor Holdings L.P., KKR Group Assets Holdings III L.P. as the sole member of KKR Harbor Holdings GP LLC, KKR Group Assets III GP LLC, as the general partner of KKR Group Assets Holdings III L.P., KKR Group Partnership L.P., as the sole member of KKR Group Assets III GP LLC, KKR Group Holdings Corp., as the general partner of KKR Group Partnership L.P., KKR Group Co. Inc., as the sole shareholder of KKR Group Holdings Corp., KKR & Co. Inc., as the sole shareholder of KKR Group Co. Inc., KKR Management LLP, as the Series I preferred stockholder of KKR & Co. Inc., and Messrs. Henry R. Kravis and George R. Roberts, as the founding partners of KKR Management LLP, may be deemed to be the beneficial owners of the securities reported herein as being held directly by HCRx Investments HoldCo, L.P.
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The principal business address of each of the entities and persons identified in the paragraphs above, except Mr. Roberts, HCRx Investments HoldCo, L.P., HCRx Master GP, LLC and Healthcare Royalty Management, LLC, is c/o Kohlberg Kravis Roberts & Co. L.P., 30 Hudson Yards, New York, NY 10001. The principal business address for Mr. Roberts is c/o Kohlberg Kravis Roberts & Co. L.P., 2800 Sand Hill Road, Suite 200, Menlo Park, CA 94025. The principal business address of HCRx Investments HoldCo, L.P., HCRx Master GP, LLC and Healthcare Royalty Management, LLC is 300 Atlantic Street, Suite 600, Stamford, CT 06901. Mr. Satvat is a member of our Board of Directors and serves as an executive of Kohlberg Kravis Roberts & Co. L.P. and/or one or more of its affiliates. Each of Messrs. Kravis, Roberts and Satvat and each of the entities and persons described in this footnote as a result of any sole member, general partner, sole shareholder, preferred stockholder or founding partner relationship, as applicable, disclaims beneficial ownership of the shares held by KKR Genetic Disorder L.P. and HCRx Investments HoldCo, L.P. The principal business address of Mr. Satvat is c/o Kohlberg Kravis Roberts & Co. L.P., 2800 Sand Hill Road, Suite 200, Menlo Park, CA 94025.
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(2)
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TSSP Sub-Fund HoldCo, a Delaware limited liability company ("Sub-Fund Holdco") is the sole member of TAO SPV GP, LLC, a Delaware limited liability company, which is the manager of Chinotto Investments, LLC, a Delaware limited liability company ( "Chinotto"), which directly holds the securities reported herein. Sub-Fund Holdco is managed by its sole member, whose managing member is Alan Waxman. Because of their relationship to Chinotto, Sub-Fund Holdco and Mr. Waxman may each be deemed to beneficially own the securities held by Chinotto. Each of Sub-Fund HoldCo and Mr. Waxman disclaims beneficial ownership of the securities held by Chinotto except to the extent of their pecuniary interest therein.
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(3)
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Consists of 4,589,611 shares of common stock directly owned by Aisling Capital IV, LP ("Aisling") and held indirectly by Aisling Capital Partners IV, LP ("Aisling GP"), as general partner of Aisling, Aisling Capital Partners IV LLC ("Aisling Partners"), as general partner of Aisling GP, and each of the individual managing members of Aisling Partners. The individual managing members (collectively, the "Managers") of Aisling Partners are Dr. Andrew Schiff and Steve Elms. Aisling GP, Aisling Partners and the Managers share voting and dispositive power over the shares directly held by Aisling. Each of Aisling GP, Aisling Partners and the Managers may be deemed to be the beneficial owner of the securities listed above only to the extent of its pecuniary interest therein. The above information shall not be deemed an admission that any of Aisling GP, Aisling Partners or any of the Managers is the beneficial owner of any securities reported herein. The address of the principal business offices of each of these entities and individuals is 489 Fifth Avenue, 10th Floor, New York, NY 10017.
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(4)
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Assumes that the Selling Stockholders dispose of all of their respective shares of common stock covered by this prospectus and do not acquire beneficial ownership of any additional shares of common stock. The registration of these shares of common stock does not necessarily mean that the Selling Stockholders will sell all or any portion of their respective shares of common stock covered by this prospectus.
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an underwritten offering;
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ordinary brokerage transactions and transactions in which the broker-dealer solicits purchasers;
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block trades in which the broker-dealer will attempt to sell the shares as agent but may position and resell a portion of the block as principal to facilitate the transaction;
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purchases by a broker-dealer as principal and resale by the broker-dealer for its account;
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an exchange distribution in accordance with the rules of the applicable exchange;
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privately negotiated transactions;
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settlement of short sales entered into after the effective date of the registration statement of which this prospectus is a part;
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broker-dealers may agree with the Selling Stockholders to sell a specified number of such shares at a stipulated price per share;
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through the writing or settlement of options or other hedging transactions, whether such options are listed on an options exchange or otherwise;
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a combination of any such methods of sale; and
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any other method permitted pursuant to applicable law.
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our Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on February 24, 2026;
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our Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, filed with the SEC on May 7, 2026;
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our Definitive Proxy Statement on Schedule 14A (other than information furnished rather than filed), filed with the SEC on April 24, 2026;
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our Current Reports on Form 8-K filed with the SEC on January 12, 2026 (with respect to Item 8.01 only), January 21, 2026, February 12, 2026, March 30, 2026, May 7, 2026 (with respect to Item 8.01 only), May 8, 2026, May 13, 2026, May 27, 2026, June 26, 2026, July 2, 2026 (with respect to Items 1.01, 3.02, 3.03, and 5.03 only), and July 22, 2026 (in each case, other than information furnished rather than filed); and
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the description of our common stock contained in Exhibit 4.3 to our Annual Report on Form 10-K for the fiscal year ended December 31, 2021, filed with the SEC on February 25, 2022, including any amendments or reports filed for the purpose of updating such description.
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Item 14.
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Other Expenses of Issuance and Distribution
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SEC registration fee*
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$75,600.80
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Legal fees and expenses
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$60,000.00
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Accounting fees and expenses
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$15,000.00
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Printing and miscellaneous expenses
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$5,000.00
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Total
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$155,600.80
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*
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$237,509.53 and $7,893.90 of the registration fees with respect to the securities registered in this registration statement were previously paid on the Registrant's registration statements on Form S-3ASR (No. 333-240147), filed on July 28, 2020 and Form S-3ASR (No. 333- 273452), filed on July 26, 2023, respectively.
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Item 15.
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Indemnification of Directors and Officers
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any breach of their duty of loyalty to our company or our stockholders;
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any act or omission not in good faith or that involves intentional misconduct or a knowing violation of law;
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unlawful payments of dividends or unlawful stock repurchases or redemptions as provided in Section 174 of the Delaware General Corporation Law; or
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any transaction from which they derived an improper personal benefit.
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Item 16.
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Exhibits
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Exhibit
Number
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Exhibit Title
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Form
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File No.
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Exhibit
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Filing Date
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Amended and Restated Certificate of Incorporation of the Registrant, as currently in effect.
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8-K
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001-38959
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3.1
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July 3, 2019
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Certificate of Amendment to the Amended and Restated Certificate of Incorporation of the Registrant.
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8-K
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001-38959
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3.1
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June 23, 2025
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Certificate of Designations, Preferences and Rights of Series A Cumulative Convertible Participating Preferred Stock of BridgeBio Pharma, Inc.
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8-K
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001-38959
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3.1
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July 2, 2026
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Amended and Restated Bylaws, as currently in effect.
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S-4
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333-249944
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3.2
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November 6, 2020
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Specimen Common Stock Certificate.
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S-1
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333-231759
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4.1
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June 24, 2019
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Form of Registration Rights Agreement, among the Registrant and certain of its shareholders.
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S-1
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333-231759
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4.3
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June 24, 2019
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Registration Rights Agreement, dated as of July 1, 2026, by and among BridgeBio Pharma, Inc. and the Purchasers identified therein.
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8-K
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001-38959
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10.2
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July 2, 2026
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5.1
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Opinion of Goodwin Procter LLP.
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Filed herewith
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23.1
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Consent of Deloitte & Touche LLP, Independent Registered Public Accounting Firm.
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Filed herewith
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23.2
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Consent of Goodwin Procter LLP (included in Exhibit 5.1 hereto).
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Filed herewith
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24.1
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Power of Attorney (included in the signature pages to this registration statement).
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Filed herewith
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107
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Filing Fee Table
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Filed herewith
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Item 17.
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Undertakings
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(a)
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The undersigned Registrant hereby undertakes:
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(1)
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To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement:
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(i)
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To include any prospectus required by section 10(a)(3) of the Securities Act;
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(ii)
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To reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in this registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price represent no more than a 20 percent change in the maximum aggregate offering price set forth in the "Calculation of Registration Fee" table in the effective registration statement; and
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(iii)
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To include any material information with respect to the plan of distribution not previously disclosed in this registration statement or any material change to such information in this registration statement;
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(2)
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That, for the purpose of determining any liability under the Securities Act, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered herein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.
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(3)
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To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.
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(4)
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That, for the purpose of determining liability under the Securities Act to any purchaser:
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(i)
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Each prospectus filed by the Registrant pursuant to Rule 424(b)(3) shall be deemed to be part of the registration statement as of the date the filed prospectus was deemed part of and included in the registration statement; and
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(ii)
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Each prospectus required to be filed pursuant to Rule 424(b)(2), (b)(5), or (b)(7) as part of a registration statement in reliance on Rule 430B relating to an offering made pursuant to Rule 415(a)(1)(i), (vii) or (x) for the purpose of providing the information required by Section 10(a) of the Securities Act shall be deemed to be part of and included in the registration statement as of the earlier of the date such form of prospectus is first used after effectiveness or the date of the first contract of sale of securities in the offering described in the prospectus. As provided in Rule 430B, for liability purposes of the issuer and any person that is at that date an underwriter, such date shall be deemed to be a new effective date of the registration statement relating to the securities in the registration statement to which that prospectus relates, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such effective date, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such effective date.
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(5)
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The undersigned Registrant hereby further undertakes that, for the purposes of determining any liability under the Securities Act, each filing of the annual reports of the Registrant pursuant to Section 13(a) or
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(6)
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Insofar as indemnification for liabilities arising under the Securities Act may be permitted to directors, officers and controlling persons of the registrant pursuant to the foregoing provisions, or otherwise, the Registrant has been advised that in the opinion of the Commission such indemnification is against public policy as expressed in the Securities Act and is, therefore, unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or controlling person of the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered, the registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by it is against public policy as expressed in the Securities Act and will be governed by the final adjudication of such issue.
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BridgeBio Pharma, Inc.
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By:
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/s/ Neil Kumar, Ph.D.
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Neil Kumar, Ph.D.
Chief Executive Officer and Director
(Principal Executive Officer)
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Signature
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Title
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Date
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/s/ Neil Kumar
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Chief Executive Officer and Director
(Principal Executive Officer)
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July 24, 2026
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Neil Kumar, Ph.D.
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/s/ Thomas Trimarchi
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President, Chief Financial Officer
(Principal Financial Officer)
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July 24, 2026
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Thomas Trimarchi, Ph.D.
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/s/ Maricel M. Apuli
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Chief Accounting Officer
(Principal Accounting Officer)
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July 24, 2026
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Maricel M. Apuli
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/s/ Eric Aguiar
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Director
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July 24, 2026
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Eric Aguiar, M.D.
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/s/ Jennifer E. Cook
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Director
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July 24, 2026
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Jennifer E. Cook
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/s/ Douglas A. Dachille
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Director
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July 24, 2026
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Douglas A. Dachille
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/s/ Ronald J. Daniels
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Director
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July 24, 2026
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Ronald J. Daniels
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TABLE OF CONTENTS
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Signature
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Title
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Date
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/s/ Andrea J. Ellis
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Director
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July 24, 2026
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Andrea J. Ellis
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|||||
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/s/ Fred Hassan
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Director
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July 24, 2026
|
|
Fred Hassan
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|||||
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/s/ Charles Homcy
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Director
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July 24, 2026
|
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Charles Homcy, M.D.
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|||||
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/s/ Andrew W. Lo
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Director
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July 24, 2026
|
|
Andrew W. Lo, Ph.D.
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|||||
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/s/ Frank P. McCormick
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Director
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July 24, 2026
|
|
Frank P. McCormick, Ph.D.
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|||||
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/s/ James C. Momtazee
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Director
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|
July 24, 2026
|
|
James C. Momtazee
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|||||
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|
/s/ Ali Satvat
|
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Director
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|
July 24, 2026
|
|
Ali Satvat
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|||||
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|||
|
/s/ Hannah Valantine
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Director
|
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|
July 24, 2026
|
|
Hannah Valantine, M.D.
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|||||
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