The Checkup by Singlecare

MARCH 8, 2024

While nonbiologic drugs are made with chemicals and have a known structure, most biologics are complex mixtures and cannot be easily identified or characterized, according to the Food & Drug Administration (FDA). Continue reading to learn more about FDA approved Humira biosimilars, which are made by various drug companies.

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European Pharmaceutical Review

APRIL 10, 2024

The recent FDA approvals of two microbiome products in the US, in November 2022 and April 2023, 1-2 represent a significant milestone, maturing the industry and paving the way for advancement and regulatory clearance of additional microbiome products in broader indications. Notably, from one donor to another, significant variations exist.

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The Checkup by Singlecare

MAY 16, 2024

From a breakthrough drug to standard-of-care treatment, Remicade (infliximab) has a storied history of treating autoimmune disease —when the immune system mistakenly identifies healthy tissues as foreign and initiates an attack. Inflectra Approved by the FDA in 2016, Inflectra (infliximab-dyyb) was the first biosimilar to Remicade.

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European Pharmaceutical Review

NOVEMBER 9, 2023

TNF-alpha is an immune modulating cytokine whose dysregulation can lead to prolonged inflammatory responses and is known to drive disease in a range of autoimmune and inflammatory disorders. MYMD-1 has shown effectiveness in pre-clinical and clinical studies in regulating the immune system.

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PharmaShots

MAY 23, 2023

The company first received the US FDA approval for its gene therapy Zynteglo in Aug 2022 for treating adult and pediatric patients with ß-thalassemia. Amongst the pipeline of gene therapy being evaluated, In Nov 2022, the company received approval for Hemgenix from the US FDA to treat Hemophilia B.

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BuzzRx

SEPTEMBER 6, 2022

Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease when your immune system attacks the lining of the joints (the synovium); this disease typically affects the joints of the hands, ankles, and knees on both sides of the body. As a result, no similar drugs from other pharmaceutical companies are available.

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Pharmaceutical Technology

FEBRUARY 1, 2023

RSV researchers at major pharmaceutical companies are currently working to develop new RSV drugs to beat future waves of RSV infection and gain the first RSV vaccine FDA approval. Pharmaceutical companies are pushing to develop drugs and vaccines for RSV with these populations in mind.

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PharmaShots

FEBRUARY 21, 2023

Market Cap: $8.46M Founded Year: 2004 Total Employees: ~4 Headquarters: Texas, United States Stock Exchange: OTCMKTS QSam Biosciences is a clinical-stage biotech company focused on developing and commercializing targeted therapeutic radiopharmaceutical products for treating cancer and related diseases.

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The Thyroid Pharmacist

OCTOBER 27, 2023

It also supports healthy detoxification and the immune system. I keep garlic oil in my natural medicine cabinet to support immunity and respiratory health during cold and flu season, or when I’m traveling. 9] It can be used to treat gut infections, yeast overgrowth, and SIBO. It has antiviral, antibacterial, and antiseptic properties.

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PharmaShots

MARCH 29, 2023

Shots: Drug patent expiry is when a patent granted to a pharmaceutical company for a particular drug expires, allowing other companies to produce and sell generic versions Like every other utility patent, pharmaceuticals also get market exclusivity of 20 years. The exact mechanism of action is uncertain.

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Pharmaceutical Technology

MAY 1, 2023

After a long period of inactivity in RSV vaccine development , two pharmaceutical companies are now approaching regulatory decisions for their RSV vaccines. An FDA decision is expected for the use of RSVPreF3 in adults of ages 60 years and above by May 3.

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pharmaphorum

NOVEMBER 4, 2022

The influenza virus is subject to constant mutations to evade host immune response, and this causes the seasonal variation in circulating strains. More positively, Pfizer/BioNTech’s vaccine was cleared for children aged five through 11 last month, having been authorised by the FDA for the over 12s in August.

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PharmaShots

MARCH 9, 2023

In 2016, she received a special career-recognition award from Fundamed Foundation (a non-profit Spanish foundation) in the category of the most influential pharmaceutical executive from Spain over the past 15 years Education: Belén is an alumnus of the University of Alcala de Henares as an MS, Ph.D.,

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The Checkup by Singlecare

SEPTEMBER 10, 2024

It is approved by the Food and Drug Administration (FDA) to treat plaque psoriasis , psoriatic arthritis , Crohn’s disease , and ulcerative colitis. According to the FDA , biological products are complex medicines made from living cells, like those from plants or animals. Wezlana (ustekinumab-auub) was FDA approved on Oct.

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The Checkup by Singlecare

JUNE 7, 2024

Remicade is made by the pharmaceutical company Janssen Biotech. Remicade has a boxed warning, also called a black box warning , the most serious warning required by the Food & Drug Administration (FDA). When starting treatment with Remicade, you may wonder what to expect. The chart below outlines both drugs.

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SingleCare

JANUARY 2, 2020

Keep up-to-date on immunizations. associate director of Clinical Pharmacy at the University of Southern California School of Pharmacy in Los Angeles says they also administer immunizations recommended by the Centers for Disease Control and Prevention (CDC) including shingles , Tdap (tetanus, diphtheria and pertussis), HPV and pneumonia.

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The Checkup by Singlecare

JUNE 7, 2024

It works on proteins that affect the immune system, which helps improve symptoms such as inflammation. Made by the pharmaceutical company Janssen Biotech, Inc., As an immunosuppressive medicine, Stelara affects the immune system, which increases the risk of infections, including serious infections that require hospitalization.

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The Checkup by Singlecare

APRIL 16, 2024

It is a biologic medication and monoclonal antibody made by the pharmaceutical company Janssen Biotech. Stelara works by blocking proteins in the immune system that cause inflammation. Stelara as a treatment for psoriasis People with psoriasis have an overactive immune system.

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The Checkup by Singlecare

AUGUST 6, 2024

Remicade: Key differences Remicade, made by the pharmaceutical company Janssen Biotech, was approved by the Food and Drug Administration (FDA) in 1998. According to the FDA , most biologics are complex mixtures that cannot be easily characterized or identified. They are also FDA approved for the same indications.

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Pharmaceutical Technology

FEBRUARY 1, 2023

Pharmaceutical companies have been working on developing vaccines and other prophylactics for respiratory syncytial virus (RSV) since its discovery in 1956. Specific mutations can occur more rapidly when a virus is under immune selective pressure by prophylactic agents including mAbs and vaccines.

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