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Friday, April 30, 2021

Janssen Applies to EMA for Approval of BCMA CAR-T Therapy for Multiple Myeloma

 The Janssen Pharmaceutical Companies of Johnson & Johnson announced today that they have submitted a Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) seeking approval of cilta-cel, an investigational B cell maturation antigen (BCMA)-directed chimeric antigen receptor T cell (CAR-T) therapy, for the treatment of patients with relapsed and/or refractory multiple myeloma.

The application is supported by positive results from the ongoing Phase 1b/2 CARTITUDE-1 study, investigating the safety and efficacy of cilta-cel.1,2 The latest results were presented at the American Society of Hematology (ASH) 2020 Annual Meeting. Clinical development is ongoing with patients enrolled globally in various studies, including sites in Europe, the United States of America, China and Japan.1,2

“Despite advances in the treatment of multiple myeloma, there remains a high unmet need, especially for patients whose disease continues to progress,” said Peter Lebowitz, M.D., PhD., Global Therapeutic Area Head, Oncology, Janssen Research & Development, LLC. “Through our collaboration with Legend Biotech, we continue to expedite the development of cilta-cel with a focus and priority on the patients who may benefit from this novel immunotherapy in the future.”

A Biologics License Application seeking approval of cilta-cel for the treatment of relapsed and/or refractory multiple myeloma is currently under review by the United States Food and Drug Administration.

https://www.businesswire.com/news/home/20210430005225/en/Janssen-Submits-Marketing-Authorisation-Application-to-the-European-Medicines-Agency-Seeking-Approval-of-BCMA-CAR-T-Therapy-Ciltacabtagene-Autoleucel-cilta-cel-for-the-Treatment-of-Relapsed-andor-Refractory-Multiple-Myeloma



Hikma receives US approval for opioid overdose treatment

 Hikma Pharmaceuticals PLC (LON:HIK) said the US Food and Drug Administration (FDA) has approved Kloxxado, its emergency treatment of known or suspected opioid overdose.

It can be used on adult and paediatric patients and contains twice as much naloxone per spray as the commonly used Narcan. It is administered in a ready-to-use nasal spray.

Drug overdose, including most commonly opioid overdose, has been described as the "leading cause of accidental death" in the US today, the pharma company said, and the situation has been exacerbated by the COVID-19 pandemic.

It added that, according to health organizations, widely prescribing and distributing naloxone may play a vital role in the fight against opioid overdose.

Kloxxado will be available in the second half of 2021.

In a separate announcement, Hikma said that current trading is in line with expectations and full-year outlook remains unchanged.

The injectables business is performing well and full-year revenue in this segment is forecast to rise 5-6% with core operating margin of 37-38%.

The generics arm is also doing well, with continued demand for COVID-19 related products and good performance from recent launches.

The group has resumed the launch of generic Advair Diskus after the FDA approved a change to the application.

Revenue in the segment will be at the top end of guidance of US$770-810mln with core operating margin of 20%.

At the annual general meeting last week, shareholders approved a 2020 final dividend of 34 cents per share, bringing the total dividend to 50 cents per share, an increase of 14% on 2019.

https://www.proactiveinvestors.com/companies/news/948157/hikma-pharmaceuticals-receives-us-approval-for-opioid-overdose-treatment-kloxxado-948157.html

WuXi AppTec First-Quarter Net Profit Jumped as Investment Income Rose

 WuXi AppTec Co. reported that its net profit more than quadrupled in the first quarter, buoyed by higher revenue and investment gains.

The China-listed pharmaceutical company said late Thursday that its first-quarter net profit rose to 1.50 billion Chinese yuan ($231.8 million), from CNY303.0 million in the same period last year.

Revenue rose to CNY4.95 billion in the first quarter from CNY3.19 billion reported last year.

Investment gains rose by CNY841.9 million during the period, the company said.

https://www.marketscreener.com/quote/stock/WUXI-APPTEC-CO-LTD-44403583/news/WuXi-AppTec-First-Quarter-Net-Profit-Jumped-as-Investment-Income-Increased-33116221/

AstraZeneca says on track to deliver on COVID shots as sales hit $275 m

 

AstraZeneca said its COVID-19 vaccine sales were $275 million in the first-quarter and it is on track to deliver 200 million doses a month from April, as better-than-expected results and a second half growth forecast boosted its shares.

Chief Executive Pascal Soriot again defended the vaccine rollout on Friday, saying that Anglo-Swedish drugmaker had not overpromised on its ability to supply shots, as he defended big cuts in deliveries that prompted a European Union lawsuit.

AstraZeneca, which has said it will not make a profit from the shot during the pandemic, was reporting financial details of distribution and sales of the vaccine it developed with Oxford University for the first time.

It said the revenue included delivery of about 68 million doses, adding that European sales were $224 million, emerging markets $43 million and $8 million in the rest of the world.

Sales of $275 million for 68 million doses equates to a price tag of around $4 per shot.

AstraZeneca was one of the leaders in the global race to develop a COVID-19 vaccine. Its cheap and easily transportable shot was hailed as a milestone in the fight against the crisis, but has since faced a series of setbacks.

"Shipments (of COVID-19 vaccines) are increasing as manufacturing improves," Soriot said during a briefing, adding that it was on track to deliver 200 million doses a month.

"We never overpromised, we communicated what we thought we would achieve at the time," he said.

AstraZeneca shares were up 3.5% at 7,654 pence at 0942 GMT, putting them on track for their best day since October. The stock, which hit record highs in July 2020 due to optimism around the vaccine, ended last year 4% lower.

The results come after a bruising start to the year as the drugmaker struggles with production of its vaccine and faces a legal battle after cutting deliveries to Europe, while regulators probe rare blood clots in people who got the shot.

"Despite the intense operational and political challenges created by AZN's COVID-19 vaccine roll out, the core business continues to perform above market expectations in a most challenging quarter, demonstrating strength across therapeutic areas and geographies," Citigroup analysts said in a note.

VACCINE RACE

Pfizer, whose COVID-19 vaccine co-developed with German partner BioNTech is several times more costly than AstraZeneca's, has forecast $15 billion for its share of sales, with analysts expecting as much as $18 billion on average.

BioNTech expects close to 10 billion euros ($12.1 billion) in revenues from committed vaccine deliveries this year but raised the prospect of more supply deals.

Moderna in February said it was expecting sales of $18.4 billion from its own vaccine this year.

Before AstraZeneca's earnings, market researcher GlobalData said it expected annual sales of $278 million this year and next for the drugmaker's coronavirus vaccine, branded Vaxzevria.

AstraZeneca said it is working as fast as possible to compile data to apply for U.S. approval. Soriot said there was nothing wrong with the data, but the dataset was very large.

RESILIENT

AstraZeneca's core business has proved resilient, with the drugmaker sticking to its forecast for 2021 on Friday and predicting better times ahead.

This guidance does not include any impact from sales of the vaccine and its $39 billion purchase of Alexion, which is expected to close in the third quarter.

Total revenue of $7.32 billion for the three months to March exceeded analysts' expectations of $6.94 billion, while core earnings of $1.63 cents per share beat a consensus of $1.48.

Quarterly sales growth was driven by best-selling lung cancer drug Tagrisso, up 17% to $1.15 billion, while revenues from heart and diabetes drug Farxiga jumped to a better-than-expected $625 million, on new prescriptions for heart failure.

https://www.marketscreener.com/news/latest/AstraZeneca-says-on-track-to-deliver-on-COVID-shots-as-sales-hit-275-million--33115067/

Thursday, April 29, 2021

Guidance on treatment for rare blood clots, low platelets tied to COVID-19 vaccine

 Last Friday, the Centers for Disease Control and Prevention (CDC) and the U.S. Food & Drug Administration (FDA) lifted the pause in administration of the Johnson & Johnson (Janssen) COVID-19 vaccine in the U.S. The temporary pause was due to reports of a serious condition called cerebral venous sinus thrombosis (CVST), which refers to blood clots in the brain's veins—not in the arteries, as is the case for most strokes—in combination with thrombocytopenia (low blood platelet count). CVST and thrombocytopenia together is called thrombosis-thrombocytopenia syndrome (TTS). When TTS is linked to receiving a COVID-19 vaccine, it is called vaccine-induced immune thrombotic thrombocytopenia (VITT). CVST has also been associated with cases of TTS in adults who received the AstraZeneca COVID-19 vaccine available in Europe, according to the European Medicines Agency, the agency responsible for the scientific evaluation, supervision and safety of medicines in the European Union.

The American Heart Association/American Stroke Association Stroke Council Leadership convened quickly to provide important guidance about CVST, TTS and VITT—the signs and symptoms and the best treatment options. The special report, "Diagnosis and Management of Cerebral Venous Sinus Thrombosis with Vaccine-Induced Thrombotic Thrombocytopenia," published today in Stroke, a journal of the American Stroke Association, a division of the American Heart Association.

"COVID-19 infection is a significant risk factor for CVST. A preliminary analysis of U.S. data during the COVID-19 pandemic, available online, preprint on April 15, 2021, found that the risk of CVST due to infection with COVID-19 is 8-10 times higher than the risk of CVST after receiving a COVID-19 ," said Karen L. Furie, M.D., M.P.H., lead author of the special report, chair of the department of neurology at The Warren Alpert Medical School of Brown University, and chief of neurology at Rhode Island Hospital, The Miriam Hospital and Bradley Hospital in Providence, Rhode Island. "The public can be reassured by the CDC's and FDA's investigation and these statistics—the likelihood of developing CVST after a COVID-19 vaccine is extremely low. We urge all adults to receive any of the approved COVID-19 vaccines."

The analysis included data from 59 health care organizations, totaling 81 million patients, more than 98% of whom were in the U.S. Among the nearly 514,000 patients in the database who were diagnosed with COVID-19 infection from January 20, 2020 through March 25, 2021, 20 patients were diagnosed with CVST. This data was compared to the incidence of CVST in adults who received either the Pfizer or Moderna COVID-19 vaccine before March 25, 2021, excluding those who had previously been diagnosed with COVID-19. No cases of thrombocytopenia (low platelets) were diagnosed among almost 490,000 vaccinated adults.

"CVST blood clots are very rare adverse events. We recommend immediate screening of all patients who arrive in the ER with a suspected clot—did they receive a COVID-19 vaccine during the recent weeks prior to this event?" said Furie. "Patients who present with the symptoms of CVST or blood clots and who recently received the COVID-19 vaccine should be treated using non-heparin anticoagulants. No heparin products in any dose should be given for suspected CVST, TTS or VITT. With the right treatment, most patients can have a full recovery after CVST, TTS or VITT."

CVST is an extremely rare but serious type of stroke caused by a blood clot in a part of the brain known as the venous sinus, involving veins that carry blood away from the brain. CVST clot symptoms are very similar to several other neurological conditions, and the symptoms can include severe headache; blurry vision; fainting or loss of consciousness; weakness; sensory changes; confusion or trouble speaking; seizures; ; leg pain; difficulty breathing or shortness of breath. CVST occurs in the veins of the brain; blood clots may also occur in other blood vessels, like those in the legs, lungs or abdomen. Among the cases reported in the U.S., the most common symptoms were severe headaches; vomiting; back pain; fatigue; weakness or the inability to move one side of the body (hemiparesis); inability to speak or understand speech (aphasia); loss of consciousness; and abdominal pain.

If associated with the COVID-19 vaccine, cases of TTS/VITT occurred several days up to 2-1/2 weeks after being vaccinated with the Johnson & Johnson (Janssen) COVID-19 vaccine in the U.S., or up to 3-1/2 weeks after receiving the AstraZeneca COVID-19 vaccine in Europe.

The CDC and FDA's report on April 23, 2021, confirms the agencies investigated 15 reported cases of TTS in the U.S., in women ages 18-59 years, from the nearly 7 million adults who received the Johnson & Johnson COVID-19 vaccine before the temporary pause on April 13, 2021. The European Medicines Agency's investigation, reported on April 7, 2021, lists 62 cases of CVST, among adults ages 22-60 years, mostly women, from the more than 25 million people who received the AstraZeneca COVID-19 vaccine throughout the European Union .

The special report from the Stroke Council leaders details treatment for suspected CVST, TTS or VITT:

  • All patients with suspected CVST due to a COVID-19 vaccine should be treated with non-heparin anticoagulants such as argatroban, bivalirudin, danaparoid, fondaparinux or a direct oral anti-coagulant (DOAC). No heparin products in any dose should be given.
  • Magnetic Resonance Imaging with a venogram (MRI/MRV) or computed tomography with venogram (CT/CTV) is recommended to accurately detect and diagnose CVST.
  • Blood tests should include a CBC (Complete Blood Count) plus:
  • platelet count—to determine the number of platelets per liter of blood;
  • a peripheral smear—examination under a microscope to count the number of various types of blood cells and if they appear normal;
  • a prothrombin time—to measure how long it takes the blood to clot;
  • a partial thromboplastin time—a measurement of how long it takes the blood to clot, specifically measuring for these clotting factors: factor VIII, factor IX, factor 1V and factor XII;
  • a fibrinogen test—to measure for the presence of fibrin, a protein found in the blood that indicates that blood clotting has been activated;
  • a D-dimer test—to measure for the presence of D-dimer, a small protein that's made when blood clots are dissolving in the body; and
  • a PF4 antibody ELISA test—to test for PF4 antibodies, which the body sometimes creates in the blood to fight against the anticoagulant heparin.
  • Anticoagulation treatment doses may need to be tailored if platelet counts are extremely low (<20,000/mm3) or if there is low fibrinogen.
  • Anticoagulants should be used to treat CVST even if there is a secondary hemorrhage in the brain in order to prevent progressive thrombosis and to control bleeding.
  • Platelet transfusion should be avoided.
  • Once platelet counts return to normal (150,000 to 450,000/mm3), most patients can be transitioned to an oral anticoagulant if there are no contraindications.
  • The authors note that based on their evaluation of the American Society of Hematology's recommendations and two recently published studies, individual patient factors should be considered regarding the use of a direct oral anticoagulant (DOAC) or a vitamin K agonist (VKA) after there is full platelet count recovery.
  • The authors recommend all cases of thrombosis after a COVID-19 vaccine be reported to the U.S. Department of Health and Human Services Vaccine Adverse Event Reporting System: https://vaers.hhs.gov/reportevent.html. This data will be important to understanding the incidence of CVST, TTS and VITT.
  • There is still much to be investigated:
  • Are there any preexisting conditions that may predispose someone to CVST or VITT?
  • What is the true prevalence and risk of PF4 antibodies, low platelet count and CVST after the COVID-19 vaccine?
  • Since there is currently no data about people who did not develop CVST, TTS or VITT after a COVID-19 vaccine for comparison, it is not possible to definitively state that the vaccine is the cause of the PF4 antibodies, low platelet count (thrombocytopenia) or blood clots (thrombosis).

"We are learning the various intricacies of COVID-19 live, in real-time with the patients we see in our hospitals every day. CVST is extremely rare, however, further research and investigation are necessary as the pandemic continues. We will need data and robust research on the people who did not develop  after the vaccine, too, so that we can fully understand the molecular and cellular mechanisms underlying CVST related to COVID-19 infection or after vaccination," concluded Furie.

The following statement reflects the views of the American Heart Association/American Stroke Association and its science leaders.

"The American Heart Association continues to urge everyone to receive a COVID-19 vaccine as soon as they can. We concur with the CDC's and FDA's recommendations for people who receive the Johnson & Johnson (Janssen) vaccine—if they develop severe headache, abdominal pain, leg pain or shortness of breath within 3 weeks of receiving the vaccine, they should quickly contact their health care professional.

COVID-19 has disproportionately negative effects on older adults; people with underlying medical conditions; and Black, LatinX and American Indian/Alaska Native people. The American Heart Association strongly encourages everyone to get vaccinated with an approved COVID-19 vaccine. In particular, people with cardiovascular risk factors such as high blood pressure, obesity and type 2 diabetes, those with heart disease, and heart attack and stroke survivors should get vaccinated as soon as possible because they are at much greater risk of a negative outcome from the virus than they are from the vaccine.

We are confident the benefits of vaccination far exceed the very small, rare risks. The risks of vaccination are also far smaller than the risks of COVID-19 and its potentially fatal consequences.

We recommend people who have medical conditions, especially those with the propensity for  clotting, consult with a health care professional before seeking vaccination to discuss the very rare potential increased risks.

In addition, the Association reiterates the importance of handwashing, social distancing and wearing masks as vaccinations continue, particularly for people at high risk of infection and/or severe COVID-19. These simple precautions remain crucial to protecting people from the virus that causes COVID-19. They also are crucial to getting us all back to normal activities.

Individuals should refer to their local and state health departments for specific information about when and where they can get vaccinated. We urge everyone to get vaccinated."

More information: Diagnosis and Management of Cerebral Venous Sinus Thrombosis with Vaccine-Induced Thrombotic Thrombocytopenia, Stroke (2021). DOI: 10.1161/STROKEAHA.121.035564

https://medicalxpress.com/news/2021-04-guidance-treatment-rare-blood-clots.html

California considers allowing adults to add parents to health insurance

 California has issued a policy proposal stating that adults should be allowed to add their parents to their health insurance plans. 

If the proposal, which passed its first committee hearing in the state legislature April 27, becomes a law, California will be the only state to allow this, according to NBC News

State lawmakers suggested that allowing parents to be claimed as dependents by their children will be beneficial in the wake of the pandemic. However, business groups said the bill would only increase employer premiums and minimize healthcare affordability.

Parents will only be eligible for the policy if they rely on their children for at least 50 percent of their support, the article said.

https://www.beckershospitalreview.com/payer-issues/california-considers-allowing-adults-to-add-parents-to-health-insurance.html

CHS, HCA, Tenet and UHS patient volume trends in Q1

 Four major for-profit hospital operators have posted patient volume results for the first quarter of 2021: 

1. Franklin, Tenn.-based Community Health Systems reported that its consolidated operating results for the first quarter of 2021 reflect a 14 percent decrease in admissions and a 15.8 percent decrease in adjusted admissions, compared with the same period last year. On a same-facility basis, admissions dipped 4.9 percent in the first quarter of 2021, and adjusted admissions decreased 7.2 percent, compared to the same period in 2020.  

2. Nashville, Tenn.-based HCA Healthcare said same-facility admissions declined 4.2 percent, and same-facility equivalent admissions declined 6.5 percent in the first quarter of 2021, compared to the same period a year prior. Same-facility emergency room visits declined 18.4 percent year over year, while same-facility inpatient surgeries declined 5.4 percent, and same-facility outpatient surgeries climbed 2.3 percent year over year. 

3. Dallas-based Tenet Healthcare said same-hospital admissions decreased 10.9 percent in the first quarter of 2021 compared to the first quarter of 2020. Same-hospital adjusted admissions — representing actual patient admissions adjusted to include outpatient services at its hospitals — decreased 13.7 percent year over year. When compared to the same period last year, Tenet noted that the headwinds from the COVID-19 pandemic weren't felt primarily until the latter half of March 2020. Its first-quarter results in 2021 were also affected by a winter storm in February and ongoing COVID-19 challenges. 

4. King of Prussia, Pa.-based Universal Health Services said adjusted admissions (adjusted for outpatient activity) at its acute care hospitals decreased 12.1 percent in the first quarter of 2021, compared to the same period a year prior. Adjusted patient days decreased 0.7 percent year over year at its acute care hospitals. UHS said adjusted admissions at its behavioral healthcare facilities on a same-facility basis decreased 4.9 percent, and adjusted patient days decreased 3.8 percent in the first quarter of 2021, compared to the first quarter of last year.

https://www.beckershospitalreview.com/patient-flow/chs-hca-tenet-and-uhs-patient-volume-trends-in-q1.html