Oseltamivir

Onconova Therapeutics, Inc. and Trawsfynydd Therapeutics, Inc. Announce Business Combination to Form Traws Pharma, Inc, a Best-in-Class Virology and Oncology Company

Retrieved on: 
tisdag, april 2, 2024

Combined board to be led by Executive Chairman Iain Dukes DPhil (OrbiMed) along with Nikolay Savchuk, Ph.D. (Torrey Pines)

Key Points: 
  • Combined board to be led by Executive Chairman Iain Dukes DPhil (OrbiMed) along with Nikolay Savchuk, Ph.D. (Torrey Pines)
    Companies to host joint webcast, April 2, 2024 at 8:30 a.m.
  • Under the terms of the agreement, Onconova acquired 100% of Trawsfynydd’s outstanding equity interests.
  • These proceeds will be used to advance the Traws’ programs through multiple clinical data catalysts and complete the dose ranging study for narazaciclib.
  • Topline data are expected H2 2024
    Phase 2 study planned to be initiated in H2 2024.

Cocrystal Pharma Highlights its Novel Inhaled and Oral Influenza A Antiviral CC-42344 at the World Vaccine Congress West Coast

Retrieved on: 
onsdag, november 29, 2023

In his presentation, “Taking a new route: Development of novel inhaled and oral influenza antiviral, CC-42344,” Cocrystal President and co-CEO Sam Lee, PhD discussed the potential prevention and therapy of influenza infection using inhaled CC-42344.

Key Points: 
  • In his presentation, “Taking a new route: Development of novel inhaled and oral influenza antiviral, CC-42344,” Cocrystal President and co-CEO Sam Lee, PhD discussed the potential prevention and therapy of influenza infection using inhaled CC-42344.
  • Dr. Lee commented that CC-42344 exhibits superior antiviral activity compared with oseltamivir (Tamiflu®) and demonstrates a novel mechanism of action with high barrier of resistance.
  • “We are excited to accomplish another important milestone with the influenza antiviral CC-42344.
  • “Inhaled CC-42344 could be developed for both therapeutic and prophylactic influenza treatment.

I think I have the flu. Should I ask my GP for antivirals?

Retrieved on: 
tisdag, augusti 29, 2023

If you test positive for COVID and you’re eligible for antivirals, you’ll likely ask your GP for a script to protect you from severe disease.

Key Points: 
  • If you test positive for COVID and you’re eligible for antivirals, you’ll likely ask your GP for a script to protect you from severe disease.
  • So when should you make the effort to see a GP for a prescription for influenza antivirals?

What exactly is influenza?


    The flu is primarily a viral infection of the respiratory system that can spread through sneezing, coughing, or touching contaminated objects then touching your nose or mouth. Common symptoms include headache, sore throat, fever, runny or blocked nose and body aches that last a week or more. Influenza is actually a group of viruses, divided into several sub-groups. Flu A and B are the most common groups that circulate in humans.

What are flu antivirals?

    • Most flu antivirals target neuraminidase, an important enzyme the virus uses to release itself from cells.
    • On the other hand, COVID antivirals work by inhibiting other parts of the viral life cycle involved in the virus replicating itself.
    • Read more:
      Should I get a flu vaccine this year?

How effective are antivirals for the flu?

    • Antivirals have the greatest effect if started 24-72 hours after symptoms.
    • In a study from the 2009 swine flu (H1N1) pandemic in the United States, treatment with antivirals (Tamiflu and Relenza) reduced the chance of needing to be hospitalised.
    • The research is less clear about whether antivirals prevent the development of flu complications such as secondary bacterial pneumonia.

Are flu antivirals becoming less effective?

    • The impact of the antiviral resistance is unclear but there is evidence indicating resistant strains can uphold their ability to replicate effectively and spread.
    • However, government agencies and surveillance programs are constantly monitoring the spread of antiviral resistance.

Antivirals can also prevent the flu if you’ve been exposed

    • Tamiflu and Relenza can also be used to prevent flu infections, if we’re exposed to the virus or come into contact with infected people.
    • Some studies suggest Tamiflu and Relenza can reduce the chance of developing symptomatic influenza by 70-90%.

So who should talk to their GP about a prescription?


    Australian guidelines recommend doctors offer antivirals to people with influenza who have severe disease or complications. Doctors can also consider treatment for people at higher risk of developing severe disease from influenza. This includes:
    • Antiviral treatment also can be considered for otherwise healthy symptomatic patients who have confirmed or suspected influenza, if they can start treatment within 48 hours of developing symptoms.
    • In some instances a doctors can make a clinical diagnosis of influenza based on the symptoms and known close flu positive contacts of the patient.
    • Read more:
      What happens in our body when we encounter and fight off a virus like the flu, SARS-CoV-2 or RSV?

SAB Biotherapeutics Presents Positive Phase 1 and 2a Data for SAB-176 Influenza Immunotherapy at ISIRV-AVG Conference

Retrieved on: 
torsdag, maj 4, 2023

SIOUX FALLS, S.D., May 04, 2023 (GLOBE NEWSWIRE) -- SAB Biotherapeutics (Nasdaq: SABS), (SAB), a clinical-stage biopharmaceutical company with a novel immunotherapy platform that produces specifically targeted, high-potency, fully-human immunoglobulin (hIgG,) antibodies, also known as fully-human polyclonal antibodies, without the need for human donors, today announced the presentation of positive safety and efficacy data from Phase 1 and 2a clinical trials of its influenza immunotherapy, SAB-176 at the AVG conference, which is hosted by the International Society for Influenza and other Respiratory Virus Diseases (ISIRV) in Seattle, Wash.

Key Points: 
  • Taking place from May 3-5, 2023, the ISIRV-AVG conference is a premier international forum for influenza research, attracting leading experts in the field from around the world.
  • SAB will conduct an oral presentation, titled “Safety and efficacy results from Phase 1 and 2a trials using an anti-Type A and B influenza immunotherapeutic,” on Thursday, May 4, at 11:20 AM PT.
  • "We are excited to present the latest positive findings on SAB-176 at the highly regarded ISIRV-AVG conference," said Eddie Sullivan, co-founder, President and Chief Executive Officer of SAB Biotherapeutics.
  • More information on SAB-176’s influenza therapeutic candidate can be found on the pipeline page of SAB’s website: sab.bio/sab-176 .

Veru Announces Preclinical Results from Expanded Sabizabulin Program into Influenza-Induced Severe Acute Respiratory Distress Syndrome and Provides Update on COVID-19 Program

Retrieved on: 
tisdag, april 4, 2023

MIAMI, FL, April 04, 2023 (GLOBE NEWSWIRE) -- Veru Inc. (NASDAQ: VERU), Veru Inc., a biopharmaceutical company focused on developing novel medicines for COVID-19 and other viral ARDS-related diseases and for oncology, today announced results from a preclinical study of sabizabulin demonstrating robust anti-inflammatory activity with improved outcomes in an Influenza-Induced Pulmonary Inflammation Mouse Acute Respiratory Distress Syndrome (ARDS) Model.

Key Points: 
  • An animal study was conducted by a team of researchers at Labcorp Early Development Laboratories, Ltd, United Kingdom.
  • The purpose of the study was to evaluate the efficacy of sabizabulin in the influenza H1N1 pulmonary inflammation mouse ARDS model.
  • Sabizabulin’s anti-inflammatory effects were previously reported in a preclinical septic shock mouse model with suppression of key cytokines responsible for severe acute respiratory distress syndrome (ARDS).
  • Accordingly, Veru is planning a double-blind randomized placebo-controlled Phase 3 clinical trial evaluating sabizabulin in hospitalized adult influenza patients at high risk for ARDS.

Genentech Announces FDA Approval of Xofluza to Treat Influenza in Children Aged Five and Older

Retrieved on: 
torsdag, augusti 11, 2022

Additionally, the FDA approved Xofluza for the prevention (post-exposure prophylaxis) of influenza in children aged five to less than 12 years of age following contact with someone with influenza.

Key Points: 
  • Additionally, the FDA approved Xofluza for the prevention (post-exposure prophylaxis) of influenza in children aged five to less than 12 years of age following contact with someone with influenza.
  • However, in the U.S. 2018-2019 influenza season, there were more than 6 million illnesses, thousands of hospitalizations and more than 100 deaths for children aged five to 17 caused by influenza.
  • Todays FDA approval provides children with a single-dose antiviral option, Xofluza, to treat influenza."
  • BLOCKSTONE evaluated Xofluza compared with placebo as a preventive treatment for household members (adults and children) who were living with someone with influenza.

Enzolytics, Inc. Discusses the Significance and Revenue Potential of Its Therapeutic Platforms with The Stock Day Podcast

Retrieved on: 
måndag, maj 16, 2022

Director and COO of the Company, Dr. Gaurav Chandra, joined Stock Day host Everett Jolly.

Key Points: 
  • Director and COO of the Company, Dr. Gaurav Chandra, joined Stock Day host Everett Jolly.
  • Dr. Chandra then elaborated on the significance of IPF Immune, citing positive results during testing against the CoronaVirus (SARS-CoV-2) strain 229e.
  • Additionally, he said that our preliminary studies with IPF-Immune have demonstrated significant in-vitro neutralization activity against Adenovirus.
  • "We have identified the conserved immutable targets in about 20 viruses, and then we went a bit further," said Dr. Chandra.

An oral antiviral drug from Korea may be a problem solver for COVID-19

Retrieved on: 
torsdag, maj 13, 2021

(See graph 1)\nThe decreased viral load in the treated group results from Niclosamide\'s antiviral mechanism in both suppressing viral replication and deactivating the virus (virucidal).

Key Points: 
  • (See graph 1)\nThe decreased viral load in the treated group results from Niclosamide\'s antiviral mechanism in both suppressing viral replication and deactivating the virus (virucidal).
  • This study may be the world\'s first in vivo evidence for anthelminthic Niclosamide to be repurposed as an antiviral drug in oral formulation.\nCNPharm\'s CP-COV03 is now expected to compete with other COVID-19 antiviral oral drug candidates, such as Pfizer\'s PF-07321332 and Merck\'s MK-4482.
  • Since Tamiflu was developed for H1N1, it has been recognized that cutting edge biotechnology is required to develop such antiviral drugs successfully.
  • CNPharm developed CP-COV03 to repurpose Niclosamide with its drug delivery system technology, and successfully improved bioavailability and the half-life of Niclosamide.

TaiGen filed US IND for its influenza antiviral TG-1000

Retrieved on: 
söndag, oktober 4, 2020

TAIPEI, Taiwan, Oct. 4, 2020 /PRNewswire/ -- TaiGen Biotechnology Company, Limited ("TaiGen") announced today that it has filed an Investigational New Drug (IND) application with the US FDA for its influenza antiviral TG-1000.

Key Points: 
  • TAIPEI, Taiwan, Oct. 4, 2020 /PRNewswire/ -- TaiGen Biotechnology Company, Limited ("TaiGen") announced today that it has filed an Investigational New Drug (IND) application with the US FDA for its influenza antiviral TG-1000.
  • TG-1000 is a novel pan-influenza antiviral, which interrupts viral replication and transmission via a cap-snatching mechanism and is able to do this effectively against influenza-A, influenza-B, avian flu H7N9, and Tamiflu-resistant viruses.
  • The first US patent for TG-1000 was successfully prosecuted and granted by the United States Patent and Trademark Office on Jan 14th, 2020.
  • TaiGen Biotechnology is a leading research-based and market-driven biotechnology company in Taiwan with a wholly-owned subsidiary in Beijing, China.

Whistleblower Lawsuit: Tamiflu Maker Won $1.4B Contract after Deceiving the FDA about Drug's Pandemic Effectiveness

Retrieved on: 
måndag, juni 29, 2020

At best, studies have found that Tamiflu might slightly shorten the duration of flu symptoms.

Key Points: 
  • At best, studies have found that Tamiflu might slightly shorten the duration of flu symptoms.
  • And worse, because Tamiflu doesn't prevent infections, Roche sold a drug that creates asymptomatic carriers that could worsen a pandemic much like those feared today in the Covid-19 pandemic."
  • The federal Food and Drug Administration repeatedly denied Roche's efforts in the early 2000s to approve Tamiflu for pandemic use.
  • The firm's qui tam / whistleblower practice group specializes in actions under the federal and state False Claims Acts and other whistleblower laws.