View ValuationVaxart 향후 성장Future 기준 점검 0/6Vaxart 의 수익과 수익은 각각 연간 65.4% 및 28.2% 감소할 것으로 예상됩니다 while EPS는 연간 25.8% 만큼 쇠퇴할 것으로 예상됩니다.핵심 정보-28.2%이익 성장률-25.82%EPS 성장률Biotechs 이익 성장23.7%매출 성장률-65.4%향후 자기자본이익률n/a애널리스트 커버리지Low마지막 업데이트01 Jun 2026최근 향후 성장 업데이트업데이트 없음모든 업데이트 보기Recent updates공고 • Jul 30Vaxart, Inc. to Report Q2, 2026 Results on Aug 06, 2026Vaxart, Inc. announced that they will report Q2, 2026 results After-Market on Aug 06, 2026공고 • Jul 07Vaxart Reports Topline 12-Month Safety Data from the 400-Participant Sentinel Safety Cohort of the Phase 2B Clinical Trial of Its Oral Pill Covid-19 VaccineVaxart reported topline data from the approximately 400-participant sentinel safety cohort of its Phase 2b clinical trial evaluating the Company’s oral pill COVID-19 vaccine candidate against an approved mRNA vaccine comparator. Participants in this safety cohort received Vaxart’s oral pill vaccine (201 participants dosed) or an approved mRNA vaccine (199 participants dosed) targeting the XBB strain of SARS-CoV-2, the virus that causes COVID-19. No vaccine-related serious adverse events (SAEs) or sustained Grade 3 or higher adverse events (AEs) were reported in either arm of the study. Data from the complete study, comprising the 400 dosed participants in the sentinel safety cohort and approximately 5,000 dosed participants in the main cohort, are currently anticipated in 2027. Participants in the main cohort received vaccines targeting the KP.2 viral strain prevalent at the time cohort dosing was initiated. Key topline 12-month results from the 400-participant sentinel safety cohort (201 oral vaccinees and 199 mRNA vaccinees) include: No vaccine-related serious adverse events (SAEs) or sustained Grade 3 or higher AEs were reported in either the oral pill vaccine or mRNA arms of the trial. The most common AEs in participants receiving the oral pill vaccine were malaise/fatigue (20.9%), headache (18.9%) and anorexia (10.0%). Fewer than 10% of participants experienced any other AE. The most common AEs in participants receiving the mRNA vaccine were injection site pain (60.3%), injection site tenderness (40.2%), malaise/fatigue (35.2%), myalgia/muscle pain (33.2%), and headache (28.6%). Arthralgia, chills, anorexia, nausea, diarrhea, and induration/swelling at the injection site were experienced by between 10-15% of participants. Fewer than 10% of participants experienced any other AE. With respect to the efficacy measure of symptomatic COVID, 33 participants in Vaxart’s oral pill vaccine arm and 30 participants in the injectable mRNA vaccine arm had symptomatic disease. Asymptomatic COVID cases were reported in 12 participants in the Vaxart oral pill arm and 12 in the mRNA vaccine arm. It should be noted that this 400-participant sentinel safety cohort was not powered to determine comparative efficacy between the two arms. Topline data from the complete study, comprising the 400 participants in the sentinel safety cohort and approximately 5,000 participants in the main cohort, are anticipated in 2027. The main cohort is designed and powered to support the planned statistical comparison of safety and relative efficacy outcomes between the two arms. Funding for this award was received under Project NextGen, an initiative by the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) in the U.S. Department of Health and Human Services (HHS), and the National Institute of Allergy and Infectious Diseases (NIAID) to accelerate and streamline the development of the next generation of innovative COVID-19 vaccines, therapeutics, and enablers. Vaxart’s project award through the Rapid Response Partnership Vehicle (RRPV) Consortium is valued at up to $344.8 million. This project has been funded in whole or in part with federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response (ASPR); Biomedical Advanced Research and Development Authority (BARDA), under Other Transaction Number: 75A50123D00005.공고 • Jul 02Vaxart, Inc. Announces Board and Committee ChangesVaxart, Inc. announced a resolution to the proxy contest in connection with the Company's 2026 Annual Meeting of Stockholders. Vaxart, Inc. initiated a search for an additional independent director to be conducted within 90 days of the conclusion of the 2026 Annual Meeting. Pursuant to a cooperation agreement between the Company and stockholders Daniel P. Houle, Mark Silverberg, DDS, MD, Matthew M. Wallace, MD, Patrice Raffy, Marc Eustace Pereira and Third Quarter Nominees Pty Ltd., the Company will work with the Stockholder Group to identify a mutually agreeable candidate to be appointed to the Board. The Stockholder Group agreed under the cooperation agreement to withdraw the director nominations of Mr. Houle, Dr. Silverberg and Dr. Wallace in connection with the 2026 Annual Meeting. The cooperation agreement additionally provided for the formation of a Stockholder Engagement Committee and a Clinical and Regulatory Affairs Committee, Board committee refreshment, including the selection of new chairs for the Nominating and Governance and Compensation Committees, the adoption of director stock ownership and resignation policies, as well as certain customary standstill, voting, engagement and other provisions.공고 • Jun 25Vaxart Provides Update to Barda Funding Award for Covid-19 Oral Pill Vaccine TrialVaxart entered into a contract modification that releases additional funding from BARDA, through a contract with Advanced Technology International, to support continuation of the Company’s ongoing Phase 2b COVID-19 oral pill vaccine candidate and advance the next phase of data analysis. Overall funding available for the trial is now approximately $345 million, a decrease of approximately $116 million from its prior modification, following an approximately 50% reduction in participants enrolled in the trial as the result of a BARDA partial termination ordered on August 5, 2025. Per the Company’s contract with Advanced Technology International, the total funding amount available to Vaxart represents an estimate of the costs that will be incurred in the study as it is currently contemplated. The latest modification allows for the release of approximately $29 million for completion of the trial and exploratory analyses to further evaluate safety and efficacy, enabling Vaxart to conduct deeper analytics from the trial data set. Vaxart intends to report 12-month data from the 400-participant Sentinel Cohort in the coming weeks and 12-month data from the 5,085-participant main cohort in the first half of 2027. Funding for this award was received under Project NextGen, an initiative led by BARDA and the National Institute of Allergy and Infectious Diseases to accelerate and streamline the development of the next generation of innovative COVID-19 vaccines, therapeutics, and enablers. This project has been funded in whole or in part with federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Advanced Research and Development Authority, under Other Transaction Number: 75A50123D00005. Vaxart’s development programs currently include pill vaccines designed to protect against coronavirus, norovirus and influenza, as well as a therapeutic vaccine for human papillomavirus.공고 • Jun 23Daniel P. Houle Issues an Investor PresentationOn June 22, 2026, Daniel P. Houle issued an investor presentation titled “A Case for Change at Vaxart”, and urged the shareholders of Vaxart, Inc to vote for his nominees; Daniel P. Houle, Mark Silverberg, and Matthew M. Wallace.공고 • Jun 10Daniel Houle Issues Letter to Shareholders of VaxartOn June 10, 2026, Daniel P. Houle issued letter to shareholders of Vaxart, Inc., seeking support to vote FOR accountability, transparency, and stockholder value by electing Daniel P. Houle, Mark Silverberg, and Matthew M. Wallace. In addition, Daniel P. Houle stating that the stockholders believe the Company possesses a unique technology platform, but stockholder value has remained compromised due to disappointing performance, declining market value, and insufficient engagement, and they call for restoring confidence, increasing transparency, improving communication, and ensuring stockholder interests are central to decision-making. Further, Daniel P. Houle stating that the nominees bring governance, healthcare, clinical, and operational expertise to strengthen oversight and accountability while supporting strategic partnerships, improved communication of the VAAST platform, rebuilding trust, and establishing committees to enhance regulatory oversight and stockholder relations. Furthermore, Daniel P. Houle in the letter concludes that the campaign is about improvement, accountability, and maximizing stockholder value, urging stockholders to vote for transparency, accountability, and stockholder representation.공고 • Jun 09Daniel P. Houle Provides Information to Shareholders of VaxartOn June 6, 2026, Daniel P. Houle posted a message on Stocktwits. Daniel P. Houle reposted the message on Stocktwits on June 7, 2026, and he anticipates reposting it daily on Stocktwits through the date of Vaxart, Inc.’s annual meeting.공고 • May 20Vaxart, Inc., Annual General Meeting, Jul 16, 2026Vaxart, Inc., Annual General Meeting, Jul 16, 2026.공고 • May 01Vaxart, Inc. to Report Q1, 2026 Results on May 07, 2026Vaxart, Inc. announced that they will report Q1, 2026 results After-Market on May 07, 2026공고 • Apr 24Vaxart, Inc. Appoints James Breitmeyer, M.D., Ph.D., to Board of DirectorsVaxart, Inc. announced the appointment of James Breitmeyer, M.D., Ph.D., to its Board of Directors. Dr. Breitmeyer brings more than 35 years of biopharmaceutical experience, having led clinical development programs resulting in eight FDA product approvals and numerous regulatory successes across the United States, Europe, and Japan. In February 2026, he joined Altay Therapeutics as CEO and Board Director, directing the advancement of the company’s pipeline of oral transcription factor therapies. He most recently served as the President and CEO of Oncternal Therapeutics, Inc., where he oversaw the clinical development of a diverse pipeline of first-in-class oncology assets. He also brings vaccine development expertise from his previous role as President of Bavarian Nordic, Inc., where he oversaw the development of cancer, infectious disease, and bioterrorism vaccines. Additionally, Dr. Breitmeyer held senior clinical leadership roles at Eli Lilly and Company and Cadence Pharmaceuticals, where he managed the transition of multiple candidates through the clinical and regulatory process toward successful commercial launch. His board experience includes previous director roles at Zogenix, Inc. and Otonomy, Inc., where he served on Audit and Compensation Committees. Previously, he held the position of President at Bavarian Nordic, Inc. and served as Executive Vice President and Chief Medical Officer at Cadence Pharmaceuticals. Dr. Breitmeyer also served as Vice President of Biotechnology at Eli Lilly and Company, where he was responsible for the corporate biotechnology pipeline. Earlier in his career, he held senior leadership roles at Applied Molecular Evolution and Serono Laboratories, where he led the development of therapies resulting in FDA approvals for Rebif® and Serostim®. Dr. Breitmeyer earned his M.D. and Ph.D. from Washington University School of Medicine. He completed postdoctoral fellowships at Harvard Medical School and the Dana-Farber Cancer Institute, where he also served as a clinical instructor.공고 • Apr 18Vaxart, Inc. announced that it expects to receive $25 million in funding from Lincoln Park Capital, LLCVaxart, Inc. announces that it has entered into a purchase agreement with Lincoln Park Capital Fund, LLC to issue common stock for gross proceeds of $25,000,000 on April 16, 2026. The Commitment Shares were issued and the Purchase Shares will be issued and sold by the Company to Lincoln Park in reliance upon the exemptions from the registration requirements of the Securities Act afforded by Section 4(a)(2) of the Securities Act and/ or Rule 506(b) of Regulation D thereunder.이익 및 매출 성장 예측BST:NB11 - 애널리스트 향후 추정치 및 과거 재무 데이터 (USD Millions)날짜매출이익자유현금흐름영업현금흐름평균 애널리스트 수12/31/2028N/A-338-301-301112/31/2027N/A-284-235-235112/31/202635611612512513/31/2026256371515N/A12/31/20252371688N/A9/30/2025148-51-30-30N/A6/30/202581-57-37-37N/A3/31/202547-58-34-33N/A12/31/202429-67-45-45N/A9/30/202417-72-51-51N/A6/30/202414-76-62-62N/A3/31/20249-82-68-67N/A12/31/20237-82-72-70N/A9/30/20234-89-92-86N/A6/30/20232-101-93-86N/A3/31/20231-108-104-94N/A12/31/20220-108-104-95N/A9/30/20220-105-88-81N/A6/30/20220-93-87-81N/A3/31/20220-80-74-68N/A12/31/20211-70-65-60N/A9/30/20211-64-60-55N/A6/30/20211-54-54-50N/A3/31/20212-47-39-37N/A12/31/20204-32-25-24N/A9/30/20208-25-17-17N/A6/30/20208-22-12-12N/A3/31/20207-19-12-12N/A12/31/201910-19N/A-13N/A9/30/20198-17N/A-15N/A6/30/20198-18N/A-16N/A3/31/20198-22N/A-9N/A12/31/20184-18N/A-15N/A9/30/20183-15N/A-11N/A6/30/20184-12N/A-8N/A3/31/20185-7N/A-16N/A12/31/20176-12N/A-10N/A9/30/20179-16N/A-9N/A12/31/20168-19N/A-12N/A12/31/20150-22N/A-15N/A더 보기애널리스트 향후 성장 전망수입 대 저축률: NB11 의 수익은 향후 3년간 감소할 것으로 예상됩니다(연간 -28.2%).수익 vs 시장: NB11 의 수익은 향후 3년간 감소할 것으로 예상됩니다(연간 -28.2%).고성장 수익: NB11 의 수익은 향후 3년간 감소할 것으로 예상됩니다.수익 대 시장: NB11 의 수익은 향후 3년간 감소할 것으로 예상됩니다(연간 -65.4%).고성장 매출: NB11 의 수익은 향후 3년 동안 감소할 것으로 예상됩니다(연간 -65.4%).주당순이익 성장 예측향후 자기자본이익률미래 ROE: NB11의 자본 수익률이 3년 후 높을 것으로 예상되는지 판단하기에 데이터가 부족합니다.성장 기업 찾아보기7D1Y7D1Y7D1YPharmaceuticals-biotech 산업의 고성장 기업.View Past Performance기업 분석 및 재무 데이터 상태데이터최종 업데이트 (UTC 시간)기업 분석2026/06/27 02:07종가2026/03/30 00:00수익2026/03/31연간 수익2025/12/31데이터 소스당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.패키지데이터기간미국 소스 예시 *기업 재무제표10년손익계산서현금흐름표대차대조표SEC 양식 10-KSEC 양식 10-Q분석가 컨센서스 추정치+3년재무 예측분석가 목표주가분석가 리서치 보고서Blue Matrix시장 가격30년주가배당, 분할 및 기타 조치ICE 시장 데이터SEC 양식 S-1지분 구조10년주요 주주내부자 거래SEC 양식 4SEC 양식 13D경영진10년리더십 팀이사회SEC 양식 10-KSEC 양식 DEF 14A주요 개발10년회사 공시SEC 양식 8-K* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.분석 모델 및 스노우플레이크이 보고서를 생성하는 데 사용된 분석 모델의 세부 정보는 당사의 GitHub 페이지에서 확인하실 수 있습니다. 또한 보고서 사용 방법에 대한 가이드와 YouTube 튜토리얼도 제공하고 있습니다.Simply Wall St 분석 모델을 설계하고 구축한 세계적 수준의 팀에 대해 알아보세요.산업 및 섹터 지표산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.분석가 소스Vaxart, Inc.는 6명의 분석가가 다루고 있습니다. 이 중 1명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.분석가기관Mayank MamtaniB. Riley Securities, Inc.Roger SongJefferies LLCJay OlsonOppenheimer & Co. Inc.3명의 분석가 더 보기
공고 • Jul 30Vaxart, Inc. to Report Q2, 2026 Results on Aug 06, 2026Vaxart, Inc. announced that they will report Q2, 2026 results After-Market on Aug 06, 2026
공고 • Jul 07Vaxart Reports Topline 12-Month Safety Data from the 400-Participant Sentinel Safety Cohort of the Phase 2B Clinical Trial of Its Oral Pill Covid-19 VaccineVaxart reported topline data from the approximately 400-participant sentinel safety cohort of its Phase 2b clinical trial evaluating the Company’s oral pill COVID-19 vaccine candidate against an approved mRNA vaccine comparator. Participants in this safety cohort received Vaxart’s oral pill vaccine (201 participants dosed) or an approved mRNA vaccine (199 participants dosed) targeting the XBB strain of SARS-CoV-2, the virus that causes COVID-19. No vaccine-related serious adverse events (SAEs) or sustained Grade 3 or higher adverse events (AEs) were reported in either arm of the study. Data from the complete study, comprising the 400 dosed participants in the sentinel safety cohort and approximately 5,000 dosed participants in the main cohort, are currently anticipated in 2027. Participants in the main cohort received vaccines targeting the KP.2 viral strain prevalent at the time cohort dosing was initiated. Key topline 12-month results from the 400-participant sentinel safety cohort (201 oral vaccinees and 199 mRNA vaccinees) include: No vaccine-related serious adverse events (SAEs) or sustained Grade 3 or higher AEs were reported in either the oral pill vaccine or mRNA arms of the trial. The most common AEs in participants receiving the oral pill vaccine were malaise/fatigue (20.9%), headache (18.9%) and anorexia (10.0%). Fewer than 10% of participants experienced any other AE. The most common AEs in participants receiving the mRNA vaccine were injection site pain (60.3%), injection site tenderness (40.2%), malaise/fatigue (35.2%), myalgia/muscle pain (33.2%), and headache (28.6%). Arthralgia, chills, anorexia, nausea, diarrhea, and induration/swelling at the injection site were experienced by between 10-15% of participants. Fewer than 10% of participants experienced any other AE. With respect to the efficacy measure of symptomatic COVID, 33 participants in Vaxart’s oral pill vaccine arm and 30 participants in the injectable mRNA vaccine arm had symptomatic disease. Asymptomatic COVID cases were reported in 12 participants in the Vaxart oral pill arm and 12 in the mRNA vaccine arm. It should be noted that this 400-participant sentinel safety cohort was not powered to determine comparative efficacy between the two arms. Topline data from the complete study, comprising the 400 participants in the sentinel safety cohort and approximately 5,000 participants in the main cohort, are anticipated in 2027. The main cohort is designed and powered to support the planned statistical comparison of safety and relative efficacy outcomes between the two arms. Funding for this award was received under Project NextGen, an initiative by the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) in the U.S. Department of Health and Human Services (HHS), and the National Institute of Allergy and Infectious Diseases (NIAID) to accelerate and streamline the development of the next generation of innovative COVID-19 vaccines, therapeutics, and enablers. Vaxart’s project award through the Rapid Response Partnership Vehicle (RRPV) Consortium is valued at up to $344.8 million. This project has been funded in whole or in part with federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response (ASPR); Biomedical Advanced Research and Development Authority (BARDA), under Other Transaction Number: 75A50123D00005.
공고 • Jul 02Vaxart, Inc. Announces Board and Committee ChangesVaxart, Inc. announced a resolution to the proxy contest in connection with the Company's 2026 Annual Meeting of Stockholders. Vaxart, Inc. initiated a search for an additional independent director to be conducted within 90 days of the conclusion of the 2026 Annual Meeting. Pursuant to a cooperation agreement between the Company and stockholders Daniel P. Houle, Mark Silverberg, DDS, MD, Matthew M. Wallace, MD, Patrice Raffy, Marc Eustace Pereira and Third Quarter Nominees Pty Ltd., the Company will work with the Stockholder Group to identify a mutually agreeable candidate to be appointed to the Board. The Stockholder Group agreed under the cooperation agreement to withdraw the director nominations of Mr. Houle, Dr. Silverberg and Dr. Wallace in connection with the 2026 Annual Meeting. The cooperation agreement additionally provided for the formation of a Stockholder Engagement Committee and a Clinical and Regulatory Affairs Committee, Board committee refreshment, including the selection of new chairs for the Nominating and Governance and Compensation Committees, the adoption of director stock ownership and resignation policies, as well as certain customary standstill, voting, engagement and other provisions.
공고 • Jun 25Vaxart Provides Update to Barda Funding Award for Covid-19 Oral Pill Vaccine TrialVaxart entered into a contract modification that releases additional funding from BARDA, through a contract with Advanced Technology International, to support continuation of the Company’s ongoing Phase 2b COVID-19 oral pill vaccine candidate and advance the next phase of data analysis. Overall funding available for the trial is now approximately $345 million, a decrease of approximately $116 million from its prior modification, following an approximately 50% reduction in participants enrolled in the trial as the result of a BARDA partial termination ordered on August 5, 2025. Per the Company’s contract with Advanced Technology International, the total funding amount available to Vaxart represents an estimate of the costs that will be incurred in the study as it is currently contemplated. The latest modification allows for the release of approximately $29 million for completion of the trial and exploratory analyses to further evaluate safety and efficacy, enabling Vaxart to conduct deeper analytics from the trial data set. Vaxart intends to report 12-month data from the 400-participant Sentinel Cohort in the coming weeks and 12-month data from the 5,085-participant main cohort in the first half of 2027. Funding for this award was received under Project NextGen, an initiative led by BARDA and the National Institute of Allergy and Infectious Diseases to accelerate and streamline the development of the next generation of innovative COVID-19 vaccines, therapeutics, and enablers. This project has been funded in whole or in part with federal funds from the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Advanced Research and Development Authority, under Other Transaction Number: 75A50123D00005. Vaxart’s development programs currently include pill vaccines designed to protect against coronavirus, norovirus and influenza, as well as a therapeutic vaccine for human papillomavirus.
공고 • Jun 23Daniel P. Houle Issues an Investor PresentationOn June 22, 2026, Daniel P. Houle issued an investor presentation titled “A Case for Change at Vaxart”, and urged the shareholders of Vaxart, Inc to vote for his nominees; Daniel P. Houle, Mark Silverberg, and Matthew M. Wallace.
공고 • Jun 10Daniel Houle Issues Letter to Shareholders of VaxartOn June 10, 2026, Daniel P. Houle issued letter to shareholders of Vaxart, Inc., seeking support to vote FOR accountability, transparency, and stockholder value by electing Daniel P. Houle, Mark Silverberg, and Matthew M. Wallace. In addition, Daniel P. Houle stating that the stockholders believe the Company possesses a unique technology platform, but stockholder value has remained compromised due to disappointing performance, declining market value, and insufficient engagement, and they call for restoring confidence, increasing transparency, improving communication, and ensuring stockholder interests are central to decision-making. Further, Daniel P. Houle stating that the nominees bring governance, healthcare, clinical, and operational expertise to strengthen oversight and accountability while supporting strategic partnerships, improved communication of the VAAST platform, rebuilding trust, and establishing committees to enhance regulatory oversight and stockholder relations. Furthermore, Daniel P. Houle in the letter concludes that the campaign is about improvement, accountability, and maximizing stockholder value, urging stockholders to vote for transparency, accountability, and stockholder representation.
공고 • Jun 09Daniel P. Houle Provides Information to Shareholders of VaxartOn June 6, 2026, Daniel P. Houle posted a message on Stocktwits. Daniel P. Houle reposted the message on Stocktwits on June 7, 2026, and he anticipates reposting it daily on Stocktwits through the date of Vaxart, Inc.’s annual meeting.
공고 • May 20Vaxart, Inc., Annual General Meeting, Jul 16, 2026Vaxart, Inc., Annual General Meeting, Jul 16, 2026.
공고 • May 01Vaxart, Inc. to Report Q1, 2026 Results on May 07, 2026Vaxart, Inc. announced that they will report Q1, 2026 results After-Market on May 07, 2026
공고 • Apr 24Vaxart, Inc. Appoints James Breitmeyer, M.D., Ph.D., to Board of DirectorsVaxart, Inc. announced the appointment of James Breitmeyer, M.D., Ph.D., to its Board of Directors. Dr. Breitmeyer brings more than 35 years of biopharmaceutical experience, having led clinical development programs resulting in eight FDA product approvals and numerous regulatory successes across the United States, Europe, and Japan. In February 2026, he joined Altay Therapeutics as CEO and Board Director, directing the advancement of the company’s pipeline of oral transcription factor therapies. He most recently served as the President and CEO of Oncternal Therapeutics, Inc., where he oversaw the clinical development of a diverse pipeline of first-in-class oncology assets. He also brings vaccine development expertise from his previous role as President of Bavarian Nordic, Inc., where he oversaw the development of cancer, infectious disease, and bioterrorism vaccines. Additionally, Dr. Breitmeyer held senior clinical leadership roles at Eli Lilly and Company and Cadence Pharmaceuticals, where he managed the transition of multiple candidates through the clinical and regulatory process toward successful commercial launch. His board experience includes previous director roles at Zogenix, Inc. and Otonomy, Inc., where he served on Audit and Compensation Committees. Previously, he held the position of President at Bavarian Nordic, Inc. and served as Executive Vice President and Chief Medical Officer at Cadence Pharmaceuticals. Dr. Breitmeyer also served as Vice President of Biotechnology at Eli Lilly and Company, where he was responsible for the corporate biotechnology pipeline. Earlier in his career, he held senior leadership roles at Applied Molecular Evolution and Serono Laboratories, where he led the development of therapies resulting in FDA approvals for Rebif® and Serostim®. Dr. Breitmeyer earned his M.D. and Ph.D. from Washington University School of Medicine. He completed postdoctoral fellowships at Harvard Medical School and the Dana-Farber Cancer Institute, where he also served as a clinical instructor.
공고 • Apr 18Vaxart, Inc. announced that it expects to receive $25 million in funding from Lincoln Park Capital, LLCVaxart, Inc. announces that it has entered into a purchase agreement with Lincoln Park Capital Fund, LLC to issue common stock for gross proceeds of $25,000,000 on April 16, 2026. The Commitment Shares were issued and the Purchase Shares will be issued and sold by the Company to Lincoln Park in reliance upon the exemptions from the registration requirements of the Securities Act afforded by Section 4(a)(2) of the Securities Act and/ or Rule 506(b) of Regulation D thereunder.