Search This Blog

Wednesday, August 19, 2020

Drug costs for COVID-19 patients plunge at U.S. hospitals, but may rise

Medication costs for COVID-19 patients hospitalized in the United States have dropped sharply since May, reflecting advances in treatment, shorter stays and use of cheaper generic drugs.

But costs may rise again as hospitals start to pay for Gilead Sciences Inc’s remdesivir.

Research by the health data firm IllumiCare and exclusively shared with Reuters found that hospitals spent $1,090 per COVID-19 patient on medication in July. That was down from $3,011 in May among more than 50 hospitals in 10 states that were analyzed.

Several factors drove down the number. The average length of stay for COVID-19 patients declined by nearly 30%, from 9.6 days in April to 6.8 days in July, the hospital data show. And the number of medications used dropped by 22%, from nearly 20 individual drugs in April to 15.4 drugs in July.

Pharmacists say some of the decrease in medications may stem from reduced use of ventilators, which require painkillers for sedation.

“We were throwing the kitchen sink at these patients and now hospitals are getting better at treating these infections,” said G.T. LaBorde, chief executive of IllumiCare, a Birmingham, Alabama-based firm that works with hospitals and analyzes their electronic medical records.

Remdesivir, which helped speed up patients’ recovery in a U.S. trial, won emergency-use authorization in May from U.S. regulators. Gilead donated early doses but has begun charging. It has said the price for commercially insured patients is $3,120 per treatment course and $2,340 for patients on Medicare.

Michael Ganio, senior director of pharmacy practice and quality at the American Society of Health-System Pharmacists, said many of the medications being used on COVID-19 patients are not “budget busters” and drug shortages have often been a bigger problem than cost.

But Ganio said pharmacy costs could increase significantly in the months ahead because of remdesivir.

Overall, many U.S. hospitals continue to face significant financial pressure from the pandemic as new infections remain high across much of the country, including in California, Florida and Texas. And health officials have warned that the upcoming flu season could further stress the healthcare system.

“As healthcare professionals, we are holding our breath for what fall will bring with flu season and COVID,” Ganio said.

In addition to remdesivir, hospital costs also may rise because of the increased use of tocilizumab, an anti-inflammatory drug widely used to treat arthritis. Hospital use jumped 29% among COVID-19 patients during July compared with the month earlier.

Tocilizumab costs more than $2,200 per patient, and is one of a class of drugs that includes Roche’s Actemra. 

The most frequently prescribed drug for COVID-19 patients was the anticoagulant enoxaparin. It was given to 50% of inpatients last month at a cost of $322 per patient, the data show.


Another treatment recently found to reduce mortality for some COVID-19 patients, the steroid dexamethasone, costs $8.78 per patient, according to IllumiCare, and it was given to 35.1% of hospitalized COVID-19 patients reviewed in July.

Overall, IllumiCare said it looked at data from March through July at health systems in 10 states, including California, Texas and Alabama. It found more than 4,000 patients who were hospitalized and under treatment primarily for a coronavirus infection, drawing on medical billing codes for respiratory infection, sepsis and related conditions.

The firm excluded some COVID-positive patients, such as pregnant women, who were hospitalized for other reasons.


Molina Healthcare and USAP in long-term agreement

Molina Healthcare (MOH +0.8%) and U.S. Anesthesia Partners (USAP) inked a three-year agreement for the latter to be in-network with Molina in Texas enabling access to additional high-quality in-network anesthesia clinicians.

USAP’s 2019 in-network strategy across U.S. led to more than 94% of its over 2.3M cases being processed as in-network.

Texas has 2.5K+ USAP clinicians serving 1M+ patients annually in 147 Texas hospitals and 152 surgery centers and other care facilities.


Convalescent plasma players under pressure on FDA hold on emergency use nod

Processors of antibody-rich convalescent plasma, derived from COVID-19 patients who have recovered from the infection, are under the gun on a delay of the expected emergency use authorization from the FDA for the treatment of COVID-19.

NIAID clinical director Dr. H. Clifford Lane says the authorization is on hold to allow for the review of more data since clinical trials have not proven that the plasma helps patients fight SARS-CoV-2.

Recent data from the largest study to date, conducted by the Mayo Clinic, were not strong enough to support emergency use approval according to top health officials, including NIAID’s Dr. Anthony Fauci. Results involving more than 35K patients showed a lower mortality rate if the convalescent plasma was administered within three days of diagnosis compared to later administration but the study has no control group so it is not possible to confirm the treatment effect. Enrollment in the study has ballooned up to an “unmanageable” level says Dr. Lane.

A study in the Netherlands was stopped after investigators saw no difference in mortality, length of hospital stay or disease severity compared to placebo.

At least 10 randomized trials in the U.S. are struggling to recruit participants since they need to be sick and the pandemic is waning in many cities.

Selected tickers: Kamada (KMDA -8.8%), Grifols (GRFS +0.1%), XBiotech (XBIT -1.8%), Cerus (CERS -1.1%), ADMA Biologics (ADMA -8.3%)


Kamada announces positive results from pediatric study of rabies treatment

Kamada Ltd. (KMDA -8.1%), along with Kedrion Biopharma, announces positive data from a U.S. post-marketing study assessing the safety of rabies treatment Kedrab (rabies immune globulin [human]) in children, the first such study conducted in a pediatric population.

The 30-subject study was conducted at two sites, one in Arkansas and the other in Rhode Island. Each participant received Kedrab for post-exposure prophylaxis (PEP) after exposure or suspected exposure to an infected animal.

Safety follow-up was up to 84 days. No serious adverse events were observed and no cases of rabies or deaths were reported.

The data have been submitted to the FDA for review and possible labeling update.

Kedrab was launched in the U.S. in April 2018. Sales last year were $31M representing ~20% market share.

Shares are down on the FDA’s hold on emergency use authorization of convalescent plasma for COVID-19.


CytoDyn requests Fast Track Approval in U.K. for COVID-19 trial

CytoDyn (OTCQB:CYDY) has provided its top-line report from its recently completed Phase 2 clinical trial for patients with mild-to-moderate COVID-19 symptoms to regulatory authorities in U.K.

The Company has requested for the regulatory pathway for Fast Track approval noting the efficacy and safety results from the Phase 2 trial.

“We are eager to see the capabilities of leronlimab in our Phase 3 clinical trial for the severe-to-critical patient population. Our enrollment is now at 182 and we are very optimistic we will reach 195 by the end of August,” stated Nader Pourhassan, Ph.D., President and CEO.



Regeneron teams with Roche to triple supply of its COVID-19 drug


The two will collaborate on developing and manufacturing REGN-COV2 – Regeneron’s investigational two-antibody “cocktail” now in late-stage clinical trials – with Regeneron handling U.S. distribution and Roche taking care of distribution outside the U.S.

That should increase overall capacity of REGN-COV2 by 3.5 times, they say, if regulators approve.

Initial study results are expected by the end of September, which could precede an emergency authorization by year-end.

The two will dedicate a certain manufacturing capacity to REGN-COV2 each year, and have already begun the technology transfer.


Takeda Pharmaceutical in talks to sell Japan consumer health unit to Blackstone

In a bid to refocus its business and reduce debt following its $59B Shire acquisition, Japan’s Takeda Pharmaceutical (NYSE:TAK) is planning to sell its domestic over-the-counter consumer healthcare unit to US fund Blackstone (NYSE:BX) for $2.85B (¥300B), reports Reuters.

Consumer healthcare unit generated FY sales of ¥64.1B, accounting for 2% of total revenue.

The talks are in the final stage and the companies plan to close the deal by the end of this month.

A Takeda spokeswoman declined to comment to Reuters on the report beyond saying it had not come from the company. A Blackstone representative was not immediately available for comment.