Regulation of tobacco by the U.S. Food and Drug Administration

National Survey Shows Drop in E-Cigarette Use Among High School Students

Retrieved on: 
Thursday, November 2, 2023

SILVER SPRING, Md., Nov. 2, 2023 /PRNewswire/ -- Today, the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention (CDC), released data from the 2023 National Youth Tobacco Survey (NYTS) on tobacco product use among U.S. youth. The findings, which were collected between March and June 2023, show that 10% of U.S. middle and high school students (2.8 million youth) reported current use of any tobacco product.

Key Points: 
  • Among U.S. high school students, current overall tobacco product use declined during 2022-2023 (16.5% to 12.6%).
  • Among high school students, declines in current use were also observed during 2022-2023 for cigars and overall combustible tobacco smoking, representing all-time lows.
  • Although a decrease in e-cigarette use was observed among high school students, among middle school students there was an increase in current overall tobacco product use (4.5% to 6.6%) and multiple tobacco product use (1.5% to 2.5%).
  • E-cigarettes remained the most commonly used tobacco product among both high school and middle school students for the 10th year in a row.

Significant Decline in E-cigarette Use Among High School Students Indicates Progress, Yet Challenges Persist in Youth Tobacco Prevention

Retrieved on: 
Thursday, November 2, 2023

WASHINGTON, Nov. 2, 2023 /PRNewswire/ -- The release of the 2023 National Youth Tobacco Survey (NYTS) marks a notable achievement in the fight against youth tobacco use. The data show a substantial reduction in current (past 30 day) e-cigarette use among high school students, dropping to 10.1% in 2023 versus 14.1% in 2022, the lowest point in almost a decade. As a result, current use of any tobacco product by high school students declined by an estimated 540,000 students, from 2.51 million in 2022 to 1.97 million in 2023.

Key Points: 
  • As a result, current use of any tobacco product by high school students declined by an estimated 540,000 students, from 2.51 million in 2022 to 1.97 million in 2023.
  • Multiple product use among middle school students has also increased with 2.5% of students reporting using more than one tobacco product, up from 1.5% in 2022.
  • With e-cigarettes remaining the most commonly used tobacco product among all youth since 2014, the survey also highlights the persistent concern of nicotine dependence.
  • Also making an impact is Truth Initiative's free digital curriculum, Vaping: Know the Truth , designed for middle and high school students.

BD Advances "One-Stick Hospital Stay" Vision with Launch of Next-Generation Needle-Free Blood Draw Technology

Retrieved on: 
Thursday, November 2, 2023

FRANKLIN LAKES, N.J., Nov. 2, 2023 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today launched new needle-free blood draw technology compatible with integrated catheters, helping to further enable the company's vision of a "One-Stick Hospital Stay."  

Key Points: 
  • New Peripheral Line Draw Solution Delivers First and Only Compatibility with Integrated Catheters, Bringing Elevated Standard of Care to More U.S.
  • Hospitals
    FRANKLIN LAKES, N.J., Nov. 2, 2023 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today launched new needle-free blood draw technology compatible with integrated catheters, helping to further enable the company's vision of a "One-Stick Hospital Stay."
  • **Clinical studies were done on previous generations of the PIVO™ Blood Collection Device and Nexiva™ Catheter System.
  • PIVO™ Pro and Nexiva™ with NearPort IV Access are the next generations of their respective product families.

RAPIDLY GROWING JARRARD INC. APPOINTS NEW VP OF STRATEGIC PARTNERSHIPS

Retrieved on: 
Friday, October 27, 2023

BRENTWOOD, Tenn. and CHICAGO, Oct. 27, 2023 /PRNewswire/ -- National healthcare strategic communications advisory firm Jarrard Inc. has added five new professionals to its team, including veteran business development expert Jennifer Dye as vice president of strategic partnerships, supporting the consultancy's Health Systems Practice.

Key Points: 
  • Jarrard Inc. has hired five new team members, each with a valuable skillset gained in various areas of healthcare.
  • Before joining Jarrard, Dye was a strategic account executive and national lab lead at Change Healthcare/Optum.
  • Previously, she was a hospital account executive at Mayo Clinic, where she led hospital and lab sales throughout the Northeast.
  • Her strategic counsel, storytelling abilities, journalism and advocacy backgrounds help clients advance their goals during periods of rapid change.

Henlius Deepens Collaboration with Intas to bring Henlius' Novel anti-PD-1 mAb Serplulimab to Europe and India

Retrieved on: 
Friday, October 27, 2023

In 2021, Henlius granted Intas the exclusive rights to develop and commercialize HLX02 in the United States (U.S.) and Canada.

Key Points: 
  • In 2021, Henlius granted Intas the exclusive rights to develop and commercialize HLX02 in the United States (U.S.) and Canada.
  • Ping Cao, Senior Vice President and Chief Business Development Officer of Henlius, said, "Henlius and Intas first entered into a collaboration in 2018.
  • Binish Chudgar, Vice-Chairman & Managing Director, Intas Pharmaceuticals Ltd., said, "We are excited to reinforce our long-standing partnership with Henlius.
  • This collaboration will further bolster Intas' global oncology portfolio, underlining our commitment to delivering innovative healthcare solutions worldwide.

U.S. FDA Grants Paige Breakthrough Device Designation for Cancer Detection in Breast Lymph Nodes

Retrieved on: 
Thursday, October 26, 2023

Paige, a global leader in end-to-end digital pathology solutions and clinical AI applications that assist in diagnosing cancer, announced today that the U.S Food and Drug Administration (FDA) has granted Breakthrough Device Designation for Paige Lymph Node1, an AI application used to detect breast cancer metastases in lymph node tissue.

Key Points: 
  • Paige, a global leader in end-to-end digital pathology solutions and clinical AI applications that assist in diagnosing cancer, announced today that the U.S Food and Drug Administration (FDA) has granted Breakthrough Device Designation for Paige Lymph Node1, an AI application used to detect breast cancer metastases in lymph node tissue.
  • Paige Lymph Node is the first AI application of its kind to receive Breakthrough Device Designation from the FDA.
  • Paige Lymph Node detects the presence of breast cancer metastases with near-perfect sensitivity3.
  • 1In the United States, Paige Lymph Node is for research use only and should not be used in diagnostic procedures.

FDA advisory panel's conclusion that oral phenylephrine is ineffective means consumers need to think twice when buying cold and flu meds

Retrieved on: 
Thursday, October 26, 2023

The ramp-up to cold and flu season is a bad time for consumers to learn that some of their most trusted go-to products don’t actually work.

Key Points: 
  • The ramp-up to cold and flu season is a bad time for consumers to learn that some of their most trusted go-to products don’t actually work.
  • The 2023 FDA advisory panel met to review growing evidence that oral phenylephrine is an ineffective treatment for nasal congestion.
  • Consumers may also question whether combination cough, cold and flu products will still be safe and effective for use at home.

The backstory

  • The most recent analysis is not the first time an FDA advisory panel has scrutinized oral phenylephrine.
  • A 2007 panel examining its use concluded that more studies were needed to make a final decision regarding the effectiveness of phenylephrine.

Safety concerns

  • No safety issues with oral phenylephrine alone were documented in the 2023 advisory panel conclusion.
  • However, researchers and advisory panel members have raised concerns about the possibility of products containing ineffective phenylephrine remaining on pharmacy shelves.
  • Even if oral phenylephrine is safe, taking an ineffective medication could cause consumers to spend money on products that work no better than a placebo.

The story behind pseudoephedrine

  • Luckily, the nonprescription oral nasal decongestant pseudoephedrine – which is known to be effective – has been commercially available for many years.
  • Pseudoephedrine is a nasal decongestant that is taken by mouth to relieve a stuffy nose.
  • If the FDA acts on the advisory committee’s conclusions that oral phenylephrine is not an effective nasal decongestant, pseudoephedrine may be the only remaining oral medication available without a prescription to treat nasal congestion.


Pseudoephedrine should not be used in doses higher than those that are recommended on the label. Use of products containing pseudoephedrine should be stopped and a health care provider consulted if dizziness, nervousness or sleeplessness occurs.
Pseudoephedrine should not be used by consumers with heart disease, high blood pressure, thyroid disease, diabetes or an enlarged prostate without talking with a health care provider like a pharmacist or a physician.
Products with pseudoephedrine should not be used while taking, or within two weeks of stopping, a prescription monoamine oxidase inhibitor, which is most commonly used to treat for depression or Parkinson’s disease.

Other treatments

  • These products are sold under the brand name Afrin and others.
  • All of these non-drug approaches can help sooth the nasal passage to provide temporary relief from congestion.
  • If symptoms of congestion continue for more than two weeks, or if signs of an infection arise, go see your doctor.


Lucas Berenbrok is part owner of the consulting company, Embarx, LLC. Colleen Culley and Karen Steinmetz Pater do not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and have disclosed no relevant affiliations beyond their academic appointment.

Marizyme CEO Delivers Business Update

Retrieved on: 
Thursday, October 26, 2023

JUPITER, FL via NewMediaWire - Marizyme, Inc. ("Marizyme" or the "Company") (OTCQB: MRZM), today provided the following business update to the stockholders and the investing public from the Company’s Chief Executive Officer, David Barthel:

Key Points: 
  • JUPITER, FL via NewMediaWire - Marizyme, Inc. ("Marizyme" or the "Company") (OTCQB: MRZM), today provided the following business update to the stockholders and the investing public from the Company’s Chief Executive Officer, David Barthel:
    “I am very pleased to bring you an update on the Company’s FDA Clearance for DuraGraft™ as well as Marizyme’s business priorities for 2024.
  • Here are our 2024 business priorities:
    DuraGraft™ U.S. commercialization including engagement of hospital integrated networks and utilization with a small direct sales force.
  • "I will continue to provide further updates on our business developments and plans in the months to come.
  • “I want to thank everyone involved in Marizyme for their support and commitment to the Company.

Integra LifeSciences Reports Third Quarter 2023 Financial Results

Retrieved on: 
Wednesday, October 25, 2023

PRINCETON, N.J., Oct. 25, 2023 (GLOBE NEWSWIRE) -- Integra LifeSciences Holdings Corporation (NASDAQ: IART), a leading global medical technology company, today reported financial results for the third quarter ending September 30, 2023.

Key Points: 
  • PRINCETON, N.J., Oct. 25, 2023 (GLOBE NEWSWIRE) -- Integra LifeSciences Holdings Corporation (NASDAQ: IART), a leading global medical technology company, today reported financial results for the third quarter ending September 30, 2023.
  • The Company reported GAAP gross margin of 57.1%, compared to 61.5% in the third quarter of 2022.
  • Adjusted EBITDA for the third quarter of 2023 was $88.1 million, or 23.0% of revenue, compared to $105.3 million, or 27.3% of revenue, in the prior year.
  • ET on Wednesday, October 25, 2023, to discuss third quarter 2023 financial results and forward-looking financial guidance.

Valneva Submits Chikungunya Vaccine Marketing Application to EMA and Announces CHMP Accelerated Assessment

Retrieved on: 
Wednesday, October 25, 2023

Saint-Herblain (France), October 25, 2023 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announces the submission of a marketing application with the European Medicines Agency (EMA) for approval of the Company’s single-shot chikungunya vaccine candidate, VLA1553.

Key Points: 
  • Saint-Herblain (France), October 25, 2023 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announces the submission of a marketing application with the European Medicines Agency (EMA) for approval of the Company’s single-shot chikungunya vaccine candidate, VLA1553.
  • Valneva was also granted accelerated assessment1 for the application by EMA’s Committee for Medicinal Products for Human Use (CHMP) based on the vaccine candidate’s “major interest for public health and therapeutic innovation”.
  • VLA1553 is currently the first and only chikungunya vaccine candidate worldwide for which regulatory review processes are underway.
  • Juan Carlos Jaramillo, MD, Chief Medical Officer of Valneva, commented, “We welcome EMA’s accelerated assessment and will work closely with them to bring this vaccine to market.