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Investopedia
Mpox Outbreak Sends Stock Of Vaccine Maker Bavarian Nordic Soaring
~1.2 mins read

Shares of Bavarian Nordic surged in Danish trading Friday as investors bought into the company with the only approved mpox vaccine in the U.S. and Europe, after the World Health Organization (WHO) declared the fast-breaking outbreak a global health emergency.

The WHO on Wednesday said the surge in mpox in African countries constituted a global pubic health emergency, its second such declaration about the disease in two years. The health organization had declared the virus, then called monkeypox, a global emergency in July 2022 but ended the call 10 months later.

The Danish firm has the only mpox vaccine approved by American, European, Canadian, and British regulators. It said Friday that it had submitted clinical data to Europe's regulators so the vaccine could be extended for use by adolescents between 12 and 17 years of age. It is currently only approved for adults 18 and over.

Sweden became the first country outside the African continent to confirm mpox in an individual who has traveled to central Africa, the WHO said. The United Nations agency said it had declared the disease a public health emergency after a surge in recent cases in the Democratic Republic of Congo and some neighboring countries and as a new, more severe strain, called clade 1b, emerged.

Bavarian Nordic stock closed up 18% in Danish trading Friday at 283.50 Danish kroner ($41.84). They surged about 48% this week.

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Instablog9ja
Don’t Let Civilisation Br3ak Your Lovely Home. Your Husband Is Your Boss — Lady Counsels Her Gender
~0.2 mins read

A lady has counseled her gender

She said don’t let civilisation br3ak your lovely home, there is nothing like 50/50 in marriage, Your husband is your boss don’t let social media brainwash you Our people are practicing selective feminism.

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Instablog9ja
Just In: FLORUISH Become The Fourth Pair Of Housemates To Be Evicted From Season 9 Of The #BBNaija Show
~0.4 mins read

DJ FLo and Rhuthiee (FLORUISH) have been evicted from the season 9 ‘No loose Guard’ edition of the Big Brother Naija Show.

They were evicted on Sunday, August 18, 2024, after their fellow house mates voted them out.

FLORUISH, STREEZE, RADICALS, and BETA were nominated for eviction by the viewers. Custodians WANNI x HANDI were only able to save one pair and they chose BETA.

FLORUISH are now the fourth pair of housemates to be evicted from the show after STREEZE, NDI NNE, and TAMI.

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Instablog9ja
FIRS Working On Executive Bill To Regulate Crypto
~1.4 mins read

The Federal Inland Revenue Service (FIRS) says an executive bill which seeks to restructure revenue administration in Nigeria, including regulation of the cryptocurrency industry, is being drafted for transmission to the national assembly.

Zacch Adedeji, FIRS chairman, spoke on Saturday at a stakeholders’ engagement with a joint committee of the national assembly in Lagos. According to a statement by Dare Adekanmbi, special adviser on media to Adedeji, the FIRS chairman said the objectives of the bill include simplifying tax laws, harmonising collection of revenue as well as seeking the replacement of obsolete tax laws with new ones in line with the current economic realities.

“By the special grace of the Almighty God, we will bring a bill for a law to overhaul the whole process of revenue administration in Nigeria. Part of what we intend to achieve with this is to harmonise revenue collection, making tax laws very simple to understand and to be in tune with our current realities,” he said.

“For example, the Stamp Duty Act was made in 1939 when there was no internet connectivity or any of the features of modern society as we have it now. Even in 1939, states and local government councils had not been created. So, we need to bring that law up to date. This is one of the reasons President Bola Tinubu set up the Taiwo Oyedele-led fiscal policy and tax reform committee to look into all these laws and make recommendations.

Today, we cannot run away from the cryptocurrency ecosystem because it is the in-thing.  But as it stands in Nigeria today, there is no law that regulates cryptocurrency operations. We need a law that regulates that area of our economy. This is why we are having this engagement with the legislators. We will regulate it in a way that is not injurious to the economic development of Nigeria. These are some of the things we are bringing together in an executive bill to overhaul revenue administration for the development of the country.”

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Healthwatch
A New Alzheimer's Drug Has Been Approved. But Should You Take It?
~3.9 mins read

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On June 7, 2021, the FDA granted accelerated approval to aducanumab (brand name Aduhelm), the first drug in 18 years for Alzheimer's disease. Since then the FDA has modified the original language of the approval to recommend that it only be used in certain patients with mild cognitive impairment or early Alzheimer's disease.

Concerns over the FDA approval of Aduhelm have led to further investigation into its safety, effectiveness, and cost. Some insurers are declining to cover it and some medical centers have decided not to prescribe it.

How does the drug work?

Aducanumab (brand name Aduhelm) is a monoclonal antibody engineered in a laboratory to stick to the amyloid molecule that forms plaques in the brains of people with Alzheimer's. Most researchers believe that the plaques form first and damage brain cells, causing tau tangles to form inside them, killing the cells. Once aducanumab has stuck to the plaque, your body's immune system will come in and remove the plaque, thinking it's a foreign invader. The hope and expectation are that, once the plaques are removed, the brain cells will stop dying, and thinking, memory, function, and behavior will stop deteriorating.

Who is a candidate for Aducanumab?

Based upon the clinical trials in which it was studied, the drug can be potentially considered for use in individuals with early-stage Alzheimer's disease. This means individuals who have Alzheimer's in its mild cognitive impairment or mild dementia stage. Individuals in this early stage of Alzheimer's may be able to function normally, or they may require a little bit of help with complicated activities like paying bills, grocery shopping, preparing meals, or balancing their checkbook. Individuals who need help with dressing, bathing, or other basic activities would be beyond the early stage and the drug would not be indicated for them.

Note that not everyone with mild cognitive impairment or mild dementia has Alzheimer's disease. There are other causes of these problems as well. To determine if Alzheimer's is present, you need to get either an amyloid PET scan or a lumbar puncture to be sure you have the amyloid plaques of Alzheimer's. Currently, a lumbar puncture is generally covered by insurance, but an amyloid PET scan (costing approximately $5,000) is not.

How do you take the drug and is it safe?

To take the drug, you need an intravenous infusion every four weeks — forever. Thirty percent of those who took the drug had a reversible swelling of the brain, and more than 10% had tiny brain bleeds. These side effects need to be watched closely by an expert neurology/radiology team who understand how to monitor for these events and know when to pause or stop the drug.

How much does it cost and how soon can I get it?

Biogen, the company that makes aducanumab, estimates its cost at $56,000 per year. It is not yet clear whether Medicare, Medicaid, or private insurance companies will pay for this medication. In its press release, Biogen noted that they are working on an agreement with the Veterans Health Administration to cover this medication for veterans enrolled in VA healthcare. Aducanumab is not currently available, but the company is working to make the drug available quickly, perhaps in a few months.

But does the drug work?

In a prior blog post I reviewed the publicly available data and the daylong FDA hearing on aducanumab. In a nutshell, there were two large clinical trials to assess effectiveness, side effects, safety, and how the drug might be used in clinical practice. One of the studies was positive, meaning that the drug worked to slow down the decline of thinking, memory, and function that is usually impossible to stop in Alzheimer's. The other large study was negative. In my view — and that of the FDA advisory panel — these results mean that we don't know if the drug works or not.

Another factor to consider is that the potential benefit — if the drug works as well as it did in the positive study — was fairly small. Looking at the two objective measures, in the positive trial, the high dose made a 0.6-point change on the 30-point Mini-Mental State Examination. On the 85-point Alzheimer's Disease Assessment Scale–Cognitive Subscale-13, the high dose made a 1.4-point change.

Discuss with your doctor

Should you or a loved one take aducanumab? You should discuss this decision with your doctor. Because we don't know if aducanumab works or not, deciding to take it is similar to deciding to participate in a clinical trial. As mentioned above, the known side effects are that 30% of people experienced reversible brain swelling and more than 10% had tiny brain bleeds. Although it does clear amyloid plaques from the brain, we don't know if it will slow down the dementia or not.

Clarity in the future

Part of the FDA's approval of aducanumab requires Biogen to conduct an additional study to try to determine if it really works. So, we may have more clarity in the future. However, this additional study will likely take three to four years, and thus its results will be too late for those trying to decide today whether to take the medication.

What everyone can do today

I am hopeful that this medication will work to slow Alzheimer's and reduce the suffering it causes individuals and their families. We should remember that the other FDA-approved medications for Alzheimer's can also be helpful (such as donepezil, galantamine, and rivastigmine), as can controlling blood pressure, engaging in aerobic exercise, eating a Mediterranean menu of foods, staying socially active, keeping a positive attitude, and using memory strategies.

Source: Harvard Health Publishing

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Instablog9ja
Davido Is The Richest Musician In Nigeria — Actor Uche Maduagwu Sets The Record Straight, Sl+ms Paulo Okoye For Saying Burna Boy Is The Richest Musician In Nigeria
~0.5 mins read

Actor Uche Maduagwu has set the record straight, as he sl+ms Paulo Okoye for saying Burna Boy is the richest musician in Nigeria.

He said Davido is the richest musician in Nigeria, even if you combine Burnaboy money spiritually and in reality together, it will still not reach #Davido own because of him wealthy family.

Davido is only into music because that’s his passion, his not doing music only to make money because he makes ten times what BURNABOY and others make in music by handling some investments in his Father business which is in Billions of Dollars, why do you think Davido can confidently give 300 Million Naira out to help others?

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