XTalks

DECEMBER 17, 2021

Xtalks is taking a look at some of the major stories and innovations of the year in the life sciences, many of which were driven by new, emerging and improved technologies. The year 2021 was all about continuing innovations in the life sciences. Life Science Innovations: Malaria and Influenza Vaccines.

Life Science 98

Life Science Vaccine Vaccination Trials 98

XTalks

OCTOBER 29, 2024

It also marks the first US approval for an oral penem antibiotic (a class of beta-lactam antibiotics with wide-ranging antibacterial activity). Orlynvah is also only the second uUTI treatment approved in the past two decades. uUTIs affect millions in the US each year and primarily affect women.

FDA Approval 105

FDA Approval Bacteria Clinical Trials Clinical Trials 105

XTalks

OCTOBER 29, 2024

It also marks the first US approval for an oral penem antibiotic (a class of beta-lactam antibiotics with wide-ranging antibacterial activity). Orlynvah is also only the second uUTI treatment approved in the past two decades. uUTIs affect millions in the US each year and primarily affect women.

FDA Approval 98

FDA Approval Bacteria Clinical Trials Clinical Trials 98

XTalks

OCTOBER 14, 2022

Whooping cough , also known as pertussis, is a highly contagious respiratory infection caused by the Bordetella pertussis bacteria. The vaccine is a Tdap vaccine (Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed) that can be administered during the third trimester of pregnancy.

FDA Approval 98

FDA Approval Vaccine Vaccination Protein 98

XTalks

DECEMBER 2, 2022

According to the FDA, the infection causes about 500,000 illnesses and is associated with 15,000 to 30,000 deaths annually in the US. difficile as certain antibiotics can disrupt the balance of bacteria in the gut, allowing bacteria like C. Last year, the company partnered with Nestlé to market the drug once approved.

FDA Approval 59

FDA Approval Bacteria Clinical Trials Clinical Trials 59

XTalks

AUGUST 2, 2022

The autoantibodies do not fight actual infection or bacteria, but rather the normal tissue in the body. In those affected by lupus, autoreactive B cells (those that react against the body), remain in the body long after the “threat” to the immune system is gone. When this behaviour is prolonged, it results in inflammation.

FDA Approval 94

FDA Approval Antibody Bacteria Protein 94

XTalks

MAY 31, 2022

Tapinarof was discovered as an outcome of investigations into the secondary metabolites of Photorhabdus luminescens, a bioluminescent, Gram-negative bacteria. There is 10 mg of tapinarof per gram of Vtama cream. XTALKS WEBINAR: All Means All: The Road to Inclusivity in Clinical Trials.

FDA Approval 98

FDA Approval Clinical Trials Clinical Trials Trials 98

XTalks

MAY 31, 2024

This novel combination antibiotic treatment is approved for complicated urinary tract infections (cUTIs), including pyelonephritis (a urinary tract infection when one or both kidneys become infected). cUTIs often require broad-spectrum antibiotics to effectively eradicate bacteria in the urinary tract. What are cUTIs? and Candida spp.

Bacteria 52

Bacteria FDA Approval Trials Drugs 52

XTalks

JULY 6, 2021

CDIs usually develop after treatments with antibiotics as they can kill off healthy bacteria in the gut in the process of targeting the pathogenic bacteria. Firmicutes microbes are an important protective species in the gut and are also involved in the life cycle of C. Related: How Sugar May Impair Brain Development in Children.

Marketing 105

Marketing Drugs Bacteria FDA Approval 105

XTalks

AUGUST 9, 2023

By focusing on the removal of excess bacteria, biofilm and bacterial toxins — the chief culprits behind eyelid symptoms — BlephEx presents a potent solution for those looking for symptom relief. This procedure, which takes just a few minutes, is crafted to address blepharitis and alleviate symptoms of dry eyes.

FDA Approval 98

FDA Approval In-Vitro Trials Bacteria 98

XTalks

JUNE 1, 2022

BONESUPPORT received market authorization from the FDA for Cerament G, the first and only bone graft with antibiotic elution that is approved for the US market. Osteomyelitis is a bone infection caused by fungi or bacteria. What was special about this latest FDA approval from the company’s (BONESUPPORT’s) commercial perspective?

Filler 98

Filler FDA Approval Production Marketing 98

XTalks

MAY 17, 2024

The settlement requires Totality to take several specific corrective actions, which include refraining from making any statements that suggest the spa’s products are genuine, FDA-approved Lilly products, and stopping the use of Eli Lilly branding in promoting any of the products.

Sales 52

Sales FDA Approval Pharmacy Production 52

XTalks

AUGUST 28, 2020

Egorov told Xtalks that, “many studies being carried out right now show that one of the major ways that people get infected with COVID or any other virus or bacteria is not by sharing the bacteria [directly] by sneezing or coughing, but by [touching surfaces], holding hands and then rubbing the nose and eyes.

Containment 111

Containment Bacteria Marketing Production 111

XTalks

AUGUST 2, 2023

Paxlovid was first authorized under the FDA Emergency Use Authorization in December 2021 ; however, it has received FDA approval on May 25, 2023. pneumoniae serotypes) replaced the company’s first pneumococcal conjugate vaccine Prevnar (PCV7, approved by the FDA in February 2000) in a February 2010 FDA approval.

Sales 98

Sales Manufacturing FDA Approval Life Science 98

XTalks

APRIL 12, 2021

Research suggests that some gut bacteria can increase levels of ?-synuclein Cala Trio is an FDA-approved device that’s worn on the wrist and that has been shown to reduce tremor power by 50 percent in patients using the device. In the life science industry, so much can change in a short period of time.

Gene Therapy 96

Gene Therapy Gene Trials Development 96

The Pharma Data

JULY 12, 2021

online issue of Nature Communications, researchers at University of California San Diego School of Medicine describe a new approach that uses machine learning to hunt for disease targets and then predicts whether a drug is likely to receive FDA approval. “Academic labs and pharmaceutical and? .”

Drugs 52

Drugs Gene Expression Big Data Gene 52

XTalks

DECEMBER 24, 2020

The pandemic propelled the life science and healthcare sectors onto center stage, and they rose to the occasion against the most unprecedented health challenge in recent times. While COVID-19 has undoubtedly been the biggest story in the life science industry in 2020, it was a busy and positive year in many other areas.

Life Science 111

Life Science Vaccine Vaccination Gene 111

XTalks

FEBRUARY 11, 2025

billion Company/developer: Gilead Sciences Date of first FDA approval: February 7, 2018 FDA-approved indications: HIV-1 Price of Biktarvy: The list price of Biktarvy is $4,216 per month. Biktarvy (Bictegravir/Emtricitabine/Tenofovir Alafenamide) Biktarvy 2023 sales: $11.85 mL) costs about $10 for a supply of 18 mL.

Sales 66

Sales FDA Approval Vaccine Vaccination 66

XTalks

MARCH 24, 2025

Due to a risk of serious infections from encapsulated bacteria, its use is limited to a Risk Evaluation and Mitigation Strategy requiring specific vaccinations. Proteinuria reductions were seen as early as 14 days and were sustained at 12 months, with similar benefits in patients switching from placebo.

Bioavailability 71

Bioavailability Immune Response Protein Bacteria 71