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The pharma industry briefing
The latest news, approvals and clinical trials you need to know about this month
Data:
News
in Numbers
$1.2trn
The value total prescription sales are expected to reach in 2024 according to Evaluate Pharma’s World Preview 2018, Outlook to 2024
52%
The percentage of the top 100 product sales biotechnology products are forecast to contribute by 2024
9th
If Takeda completes its acquisition of Shire it could be on track to become the ninth largest pharmaceutical company based on 2024 sales
$262bn
The forecast value the orphan drug market is expected to reach in 2024
20%
The percentage of the total prescription drug market forecast to be held by the orphan drug market in 2024
Data:
News
in Numbers
$1.2trn
The value total prescription sales are expected to reach in 2024 according to Evaluate Pharma’s World Preview 2018, Outlook to 2024
9th
If Takeda completes its acquisition of Shire it could be on track to become the ninth largest pharmaceutical company based on 2024 sales
52%
The percentage of the top 100 product sales biotechnology products are forecast to contribute by 2024
20%
The percentage of the total prescription drug market forecast to be held by the orphan drug market in 2024
$262bn
The forecast value the orphan drug market is expected to reach in 2024
Orion acquires sales & distribution rights for certain EC countries for Stalevo
Orion Corporation and Novartis Pharma AG have agreed that Novartis will return the sales and distribution rights in certain European countries for Parkinson’s disease drug Stalevo® to Orion.
The sales and distribution rights in certain European countries for the proprietary product Stalevo (active pharmaceutical ingredients: levodopa, carbidopa, entacapone), which has been patented and developed by Orion for the treatment of Parkinson’s disease, transferred from Novartis to Orion as of 3 December 2018.
Source: Pharmafield
CarThera raises €9m to tackle the blood-brain barrier
French company CarThera has raised €9m in its Series B funding round to help it develop ultrasound-based medical devices to treat brain disorders and overcome the challenges of the blood-brain barrier.
The funding, equivalent to $10.3m, was raised with three institutional investors, Panakès Partners, Sham Innovation Santé (advised by Turenne Capital) and Supernova Invest via its fund Supernova 2, as well as Group Arnault and historical investors.
The proceeds will be used to further advance the company’s SonoCloud technology and develop its clinical pipeline.
Source: Pharmaphorum
UTI test often fails to detect infection, say researchers
The “gold standard” test for urinary tract infections (UTIs) is not fit for purpose, according to research which suggests that it fails to diagnose most chronic sufferers.
UTIs afflict an estimated 150-200 million people around the world every year. While many, particularly young women, suffer acute attacks of cystitis, which is quickly resolved with a few days of antibiotics, chronic infection can stay with people for many years and wreak havoc with their lives.
Source: The Guardian
NIH to scrutinise private donations to scientific research projects
After halting a discredited alcohol study, officials will enforce new policies to ensure that private support does not compromise scientific integrity.
In a report, National Institutes of Health (NIH) officials said its 27 institutes must evaluate all current research projects that receive private donor support for conflicts of interest of the kind that compromised the alcohol trial. The institute directors are to report their findings to Dr Francis Collins, director of NIH, early next year.
Source: New York Times
Approvals
Juluca (dolutegravir/rilpivirine)
GSK’s single pill, two-drug regimen, for the maintenance treatment of HIV, has been granted marketing approval by Japan's Ministry of Health, Labour and Welfare
The ministry approved Juluca Combination Tablets (containing dolutegravir 50mg/rilpivirine 25mg) for the maintenance treatment of human immunodeficiency virus type 1 (HIV-1) infection
Source: GSK
Tecentriq
Swiss group Roche announced its Tecentriq immunotherapy mixed with chemotherapy has won priority review from the US FDA for treating a type of lung cancer, a potential boost to the drug that has been trailing rivals’ revenues.
The announcement comes after Roche in September said patients with untreated extensive-stage small cell lung cancer (SCLC) lived a median 12.3 months after getting the Tecentriq cocktail, compared to 10.3 months for those getting chemotherapy alone.
Source: Reuters
Tolsura (SUBA-itraconazole)
The US FDA has approved Mayne Pharma’s Tolsura 65mg capsules for the treatment of certain systemic fungal infections in adult patients.
Tolsura is indicated for the treatment of blastomycosis (pulmonary and extrapulmonary), histoplasmosis (including chronic cavitary pulmonary disease and disseminated, non-meningeal histoplasmosis) and aspergillosis (pulmonary and extrapulmonary, in patients who are intolerant of or who are refractory to amphotericin B therapy).
Source: Cision
Takhzyro (lanadelumab)
Shire has announced that the European Commission has approved its hereditary angioedema (HAE) drug Takhzyro.
Takhzyro is a subcutaneous injection indicated for routine prevention of recurrent HAE attacks in patients aged 12 years and older.
Source: Pharma Times
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