Veru Announces Appointment of Joel Batten to Lead U.S. Infectious Disease      Franchise to Focus on Hospitalized COVID-19 Patients
  MIAMI, May 18,      2022 (GLOBE NEWSWIRE) -- Veru Inc. (NASDAQ: VERU), a biopharmaceutical      company focused on developing novel medicines for COVID-19 and other viral      and ARDS-related diseases and for the management of breast and prostate      cancers, today announced the appointment of Joel Batten as Executive Vice      President and Head of its U.S. Infectious Disease Franchise effective May      23, 2022.
  Most recently Mr. Batten has been the Head of the      Respiratory Syncytial Virus (RSV) Franchise at Sobi North America where he      was responsible for the Synagis business with gross revenue of      approximately $600M and a team of over 160 employees. Mr. Batten led sales      and marketing for the RSV Franchise as well as strategy for market access,      distribution and patient access services. Prior to Sobi, he spent      approximately 20 years in a number of positions of increasing      responsibility at AstraZeneca / MedImmune and Sanofi Aventis in various      infectious disease franchises including commercial infrastructure      build-out, product launch, sales management, marketing, public health      sales, and government affairs.
  "Joel is an accomplished commercial      leader with extensive knowledge in viral infectious disease product      commercialization," said Mitchell Steiner, M.D., Chairman, President and      Chief Executive Officer of Veru Inc. "We are excited to have Joel join      Veru at such a critical juncture in our Company's history as we build on      the momentum of our positive Phase 3 sabizabulin for COVID-19 trial, our      planned EUA submission, and the transition to delivering sabizabulin, if      EUA is granted, to hospitalized COVID-19 patients at high risk for ARDS.      Joel will be the head of our newly formed U.S. Infectious Disease      Franchise and will be responsible for developing and leading all aspects      of our U.S. go-to-market strategy for sabizabulin for COVID, if      authorized, as well as planned future indications for other viral and      ARDS-related and inflammatory diseases."
  About Veru Inc.
  Veru      is a biopharmaceutical company focused on developing novel medicines for      COVID-19 and other viral and ARDS-related diseases and for the management      of breast and prostate cancers.
  A double-blind, randomized,      placebo-controlled Phase 3 COVID-19 clinical trial was conducted in      approximately 210 hospitalized COVID-19 patients with moderate to severe      COVID (>= WHO 4-supplemental oxygen) at high risk for ARDS and death. The      primary endpoint was the proportion of deaths by Day 60. Based on a      planned interim analysis of the first 150 patients randomized, the      Independent Data Monitoring Committee unanimously halted the study for      overwhelming efficacy and safety. Treatment with sabizabulin 9mg once      daily, an oral, first-in-class, new chemical entity, cytoskeleton      disruptor that has dual anti-inflammatory and antiviral properties,      resulted in a clinically meaningful and statistically significant 55.2%      relative reduction in deaths. After a pre-EUA meeting with FDA, the      Company is in the process of submitting a request for FDA emergency use      authorization. FDA granted Fast Track designation to the Company's      COVID-19 program in January 2022.
  The Company's late-stage breast      cancer development portfolio comprises enobosarm, a selective androgen      receptor targeting agonist, and sabizabulin.
  Current studies on the      two drugs include:
  -- Enrolling Phase 3 ARTEST study of enobosarm      in androgen receptor positive, estrogen receptor positive, and human      epidermal growth factor receptor two negative (AR+ ER+ HER2-) metastatic      breast cancer with AR >= 40% expression (third-line metastatic setting),      and which has been granted Fast Track designation by the FDA. -- Enrolling      Phase 3 ENABLAR-2 study of enobosarm + abemaciclib (a CDK 4/6 inhibitor)      combination in AR+ ER+ HER2- metastatic breast cancer with AR >= 40%      expression (second-line metastatic setting). The Company and Eli Lilly and      Company have entered into a clinical study collaboration and supply      agreement for the ENABLAR-2 study. Lilly is providing clinical supply of      Verzenio(R) (abemaciclib). -- Planned Phase 2b study of sabizabulin in AR+      ER+ HER2- metastatic breast cancer with AR 40% expression (third-line      metastatic setting).
  Veru's late-stage prostate cancer portfolio      comprises sabizabulin, VERU-100, a long-acting GnRH antagonist, and      zuclomiphene citrate, an oral nonsteroidal estrogen receptor agonist.
  Current      studies on these drugs include:
  -- Enrolling Phase 3 VERACITY study      in metastatic castration and androgen receptor targeting agent resistant      prostate cancer prior to IV chemotherapy. -- Enrolling Phase 2      dose-finding study of VERU-100 in advanced hormone sensitive prostate      cancer. -- Planned Phase 2b study of zuclomiphene citrate to treat hot      flashes in men with advanced prostate cancer undergoing androgen      deprivation therapy.
  Veru also has a commercial sexual health      division - Urev, the proceeds of which help fund its drug development      programs, comprised of 2 FDA approved products:
  -- ENTADFI(TM)      (finasteride and tadalafil) capsules for oral use, a new treatment for      benign prostatic hyperplasia, for which commercialization launch plans are      underway. -- FC2 Female Condom(R) (internal condom), for the dual      protection against unplanned pregnancy and the transmission of sexually      transmitted infections which is sold in the U.S. and globally.
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