Search
Close this search box.
Categories
Uncategorized

Limited Distribution Deals Announced

Announcements for newly approved specialty drugs often state that the product will be available through specialty pharmacy in limited distribution. However, the press releases rarely specify the specialty pharmacy(ies) selected as designated partner(s).

Here are three LD deals that have been recently publicly confirmed subsequent to the approvals.

Amber Specialty Pharmacy Selected to Dispense TZIELD (teplizumab), a Monoclonal Antibody Treatment to Delay Onset of Stage 3 Type 1 Diabetes in Patients with Stage 2 Type 1 Diabetes

OMAHA, Neb., — Amber Specialty Pharmacy announces that it will begin dispensing TZIELD (teplizumab), an anti-CD3 monoclonal antibody, to delay Stage 3 Type 1 Diabetes (T1D) in patients ages 8 years and older with Stage 2 T1D. Indication for individuals ages 8 years and older with Stage 2 T1D is categorized by the presence of two or more T1D-related autoantibodies and abnormal blood sugars. TZIELD™ is manufactured by Provention Bio, Inc., a New Jersey-based biopharma company.

Orsini Specialty Pharmacy Selected by Provention Bio as a Limited Distribution Partner for TZIELD

ELK GROVE VILLAGE, Ill., /PRNewswire/ — Orsini Specialty Pharmacy, a leading independent specialty pharmacy focused on rare diseases, and gene therapies, has been selected by Provention Bio, Inc. https://www.gilead.com/as a specialty pharmacy for TZIELD® (teplizumab). TZIELD is the first and only treatment indicated to delay the onset of Stage 3 type 1 diabetes (T1D) in adult and pediatric patients aged 8 years and older with Stage 2 T1D approved by the FDA.

ELAHERE Available at Biologics by McKesson

Biologics by McKesson, an independent specialty pharmacy specializing in oncology and rare disease areas, has been selected by ImmunoGen, Inc. as the sole specialty pharmacy provider for ELAHERE (mirvetuximab soravtansine-gynx) for the treatment of adult patients with folate receptor alpha (FRα)-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens.

Categories
Uncategorized

Rigel Pharmaceuticals receives FDA green light for REZLIDHIA

Rigel Pharmaceuticals recently received the green light from the FDA for their oral IDH1 inhibitor, REZLIDHIA (olutasidenib).  REZLIDHIA is indicated for treatment of acute myeloid leukemia (AML) in a difficult to treat, relapsed or refractory (R/R) patient population who have a mutation in isocitrate dehydrogenase-1 (IDH1).  Mutations of IDH1 are found in 7-14% of patients with AML and there have been few treatment options for these patients, particularly in the second line.  The FDA approval was supported by data from the open-label Phase 2 registrational study evaluating REZLIDHIA monotherapy at a dose of 150 mg twice daily in 153 mIDH1 R/R AML patients. The efficacy-evaluable population was 147 patients who initiated REZLIDHIA at least six months prior to the interim analysis cutoff date of June 18, 2021, and who had a centrally confirmed IDH1 mutation.  Acute myeloid leukemia (AML) is a rapidly progressing cancer of the blood and bone marrow that affects myeloid cells, which normally develop into various types of mature blood cells. AML occurs primarily in adults and accounts for about 1 percent of all adult cancers. The American Cancer Society estimates that in the United States alone, there will be about 20,050 new cases, most in adults, in 2022.

Relapsed AML affects about half of all patients who, following treatment and remission, experience a return of leukemia cells in the bone marrow.2 Refractory AML, which affects between 10 and 40 percent of newly diagnosed patients, occurs when a patient fails to achieve remission even after intensive treatment.3 Quality of life declines for patients with each successive line of treatment for AML, and well-tolerated treatments in relapsed or refractory disease remain an unmet need. 

REZLIDHIAprovided a complete remission (CR) combined with partial hematological recovery (CRh) within less than two months (mean time to response 1.9 months) lasting for over two years (mean duration 25.9 months) and demonstrated a CR+CRh rate of 35% in patients with over 90% of those responders in complete remission.

“The 25.9 months median duration of CR+CRh is a clinically meaningful improvement for AML patients and appears to be longer than currently available treatment options,” said Jorge E. Cortes, M.D., Director, Georgia Cancer Center, Cecil F. Whitaker Jr., GRA Eminent Scholar Chair in Cancer, and Phase 2 trial investigator. “Given the limited treatment options for adult patients with mIDH1 R/R AML, who typically have a poor prognosis, REZLIDHIA may provide an effective, new treatment option with a well characterized safety profile.”

Complete remission was achieved for over 28 months (mean 28.1 months).  Over 1/3 of patients (34%) treated with REZLIDHIAwere able to avoid platelet and/or red blood cell transfusions at 56 days and unlike other treatments in the relapsed/refractory AML space, there is no need for cardiac monitoring. REZLIDHIAhas a black box warning for differentiation syndrome which can be fatal; if suspected, differentiation syndrome should be treated with corticosteroids and hemodynamic monitoring.  

Hats off to Rigel Pharmaceuticals for getting the FDA nod just four months after acquiring the asset.  REZLIDHIAhas the potential to address an unmet need in a niche patient population typically subject to a poor prognosis.  It is motivating to see companies like Rigel invest in bringing to market therapeutic options for small, tough to treat patient populations.

Click here for the full press release from Rigel Pharmaceuticals: https://www.rigel.com/investors/news-events/press-releases/detail/349/rigel-announces-u-s-fda-approval-of-rezlidhia

Click here for full prescribing information: https://www.rezlidhia.com/downloads/pdf/REZLIDHIA-Full-Prescribing-Information.pdf

Categories
Uncategorized

FDA Approves Sub-q Tx for Multiple Myeloma – Tecvayli

Whoa….. we missed covering this FDA approval.

Way back in October the FDA approved a new subcutaneous treatment, Tecvayli from Janssen Biotech, for adult patients with relapsed or refractory multiple myeloma who have received at least four prior lines of therapy. Tecvayli is a first-in-class, bispecific T-cell engager antibody engineered to redirect body’s immune system to recognize and kill cancer cells.

Multiple myeloma is typically diagnosed in people aged between 65 and 74 and affects more men than women. According to the American Cancer Society’s estimates, close to 35,000 new cases of multiple myeloma are likely to be diagnosed in the United States this year.

The approval, however, comes with a boxed warning and will only be available through a restricted program under a REMS called the Tecvayli REMS because of the risks of cytokine release syndrome, and neurologic toxicity, including ICANS.

Tecvayli is Janssen’s fourth approved treatment for multiple myeloma. A company spokesperson said the therapy will launch with a list price of $39,500 per month, with the overall pricing ranging between $355,000 and $395,000 for a nine-to-10-month course.

Janssen has not yet announced distribution plans. Given the cost and that Tecvayli is a sub-q therapy, it is expected that one or more specialty pharmacies will be selected for a Limited Distribution program.

CLICK HERE for prescribing information

Categories
Uncategorized

Anton Health Welcomes Tara Mautone

In the spirit of continuing to elevate our client offerings, services and experiences Anton Health is proud to welcome Tara Mautone as the Executive Director of Client Services. Tara joins Anton with over 17 years of commercialization experience from a wide variety of leadership roles within both large pharmaceutical organizations and small, start-up biotech companies. This includes nearly 10 years of building a deep level of expertise in all areas of market access, leading nationally recognized commercial teams in both sales and marketing and being recognized as HBA’s Rising Star and Market Access Leader of the year.

Liz Turner, Anton Health’s VP of Operations shared, “Anton Health is committed to ensuring our clients can successfully navigate an ever-complicating market access environment. Anchored in our one-of-a-kind advisor network, we have a vision of delivering unmatched relevant, real- world solutions through the lens of the customer. Tara has been in the role of our clients responsible for developing market access strategies for pipeline assets at small start-ups and managed the pressures of increased competition in already crowded therapeutic areas. She understands how critical it is for the deliverables promised by a thought partner like Anton Health to be best-in class no matter how big or small the ask.”

We have an unrelenting desire to surpass our client’s expectations. We’re thrilled to have Tara leading the efforts for Anton Health that ensure we’ve optimized every opportunity to see this through.

Tara Mautone is a strategic commercial leader with over 17 years of pharmaceutical and biotech experience. During her career she has launched several products in multiple therapeutic areas, specializing in market access and commercialization strategy. Prior to joining Anton Health, Tara spent two years at Biosplice Therapeutics where she helped build and develop the commercial infrastructure needed to prepare for the organizations first product launch. Prior to that she spent 13 years at Daiichi Sankyo, where she held various roles in Sales Leadership, Sales Training, Market Access, Operations and ultimately, Sr. Leadership roles with broader responsibilities for the US commercial business function. Tara was recognized for her work and leadership by being named HBA’s rising star and Market Access Leader of the year. Tara graduated with a BA in Psychology from Edinboro University. She resides in Millburn, NJ with her husband Anthony, their two daughters, Giada (10) and Marcella (7) and their puppy Bruno.Tara’s phone number is 814-931-9488 and email is tara.mautone@antonhealth.com

Categories
Uncategorized

Optum Launches Specialty Fusion Platform

Optum is turning to technology to bring down special infusion spend. Others have tried a variety of ideas to achieve this goal going back to the early 2000s with limited results….. but the old saying goes….. Try…. Try…. And Try Again.

Optum is optimistic that they can deliver sustainable savings in the difficult-to-manage infusion settings where placing constraints on hospitals and physicians are often impossible. Instead, the new platform being touted by Optum, branded as Specialty Fusion, makes it ‘easier for clinicians to cut wait time for multiple treatment regimens to be approved, support navigating patient treatment plans, and optimizing health benefits’.

Perhaps one area where Specialty Fusion will help push platform adoption is in the area of cost containment. They say they can realize savings of 17%! The announcement did not address the elephant in the room, the fact that hospital infusions generally cost twice that for the same infusion in an infusion clinic or physician’s office. One would think that even greater saving could be realized by tackling that thorny issue.

As with a lot of new technology, the Specialty Fusion portal will need to be very user friendly and offer meaningful clinical and operational information to gain provider support.

————————————————————————————

Optum unveils new platform for managing specialty drug costs

Optum has launched a new solution aimed at the specialty drug market.

Specialty Fusion arms payers and providers with real-time insights into which specialty therapies are the most effective for the patient at the lowest cost. The platform leads to quicker treatment approvals for patients as well as a similar experience for providers at the point of care, Optum said in an announcement.

Internal analysis of the solution suggests it can drive cost savings of 17%.

“The average specialty patient sees more than five care providers per year, while taking more than 10 drugs on average. They often have to wait for multiple treatment regimens to be approved and need better support navigating their treatment plan and health benefits,” said Kerri Tanner, senior vice president at Optum Rx, in a statement.

“We developed a new comprehensive, benefit-agnostic solution that supports streamlined treatment decision-making for care providers, helping patients get on their therapies faster, while driving down high costs,” Tanner said.

Specialty Fusion is currently available to all large health plans, Optum said.

Specialty drugs account for an increasing amount of healthcare spending, with costs expected to reach $505 billion by 2023, Optum said. Finding ways to ensure people can access therapies that they need at a manageable cost has been of critical concern in the pharmaceutical space.

Through Specialty Fusion, providers can kickstart prior authorization through a single portal, and see comparisons for other lower-cost and clinically appropriate options for the patient. The platform is designed to reduce administrative effort and connect patients with these treatments 50% quicker, Optum said.

For example, a doctor could prescribe an immunosuppressive drug that is covered by the patient’s insurance, with a cost of about $1,200. Specialty Fusion would identify alternatives, bringing the cost down by $700 on average.

In addition, the platform arms docs with information on pharmacy networks, best sites of care, dosage management policies and other levers they can use to further lower costs.

“Managing specialty drugs at the earliest possible moment is critical to improving care, clinical outcomes and the patient experience,” said Sarah Dye, senior vice president at Optum Health, in a statement. “Optum Specialty Fusion uniquely partners with the provider to change the status quo of prior authorization, reduce their administrative pain and ultimately help them provide better care for their patients.”

Categories
Uncategorized

FDA Approves New Tx with 39 NDCs – Hemgenix

It has finally happened….. the decades’ long wait for the approval of the holy grail in hemophilia treatment….. a gene therapy that replaces the need for frequent blood factor infusions.

BUT….. the approval of this new ‘cure’ needs some explaining….. including why the new therapy was approved with….. count ‘em….. 39 NDCs.

First, this new one-and-done therapy is called Hemgenix (etranacogene dezaparvovec-drlb) and was developed by CSL Behring. 

Second, Hemgenix is indicated only for Hemophilia Type B (congenital Factor IX deficiency).

Type B represents 8,000 individuals in the US vs. Type A (congenital Factor VIII deficiency) at over 25,000.

CSL trials showed that 94% of individuals with Type B had a positive response and realized a 54% reduction in the annual bleed rate…. (not too shabby but far from a total cure). 

Third, is the little sniggly thing related to cost. 

Hemgenix will hit the market at a sizzling $3.5 million making it the world’s most expensive drug. That may stall access for patients as payers struggle to deal with the expense burden.

Fourth, here is what you’ve been waiting for……

Hemgenix was approved with 39 NDCs. 

It is available in multi-vial kits providing 100mL – 480 mL (10mL per vial) as Hemgenix requires weight-based dosing….. hence the 39 unique NDCs.

It remains to be seen how quickly (if?) Hemgenix will see strong uptake. Individuals with hemophilia are very cautious when considering any change in the factor they use due to a historical correlation with triggering inhibitor reactions. As we know, blood factor dispensing is predominantly provided by a small sub-set of specialty pharmacies nationally. It is likely that Hemgenix will be distributed directly to leading hemophilia treatment centers / hospitals due to cost and infusion management. 

CLICK HERE to access full prescribing information

Categories
Uncategorized

FDA Approves New IV Tx for Cancers – Elahere

The FDA recently approved a new infused therapy, Elahere (mirvetuximab soravtansine-gynx) from ImmunoGen Inc., indicated for the treatment of adult patients with folate receptor alpha (FRα)-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens. 

Elahere is a first-in-class antibody-drug conjugate (ADC) directed against FRα, a cell-surface protein highly expressed in ovarian cancer and is the first FDA approved ADC for platinum-resistant disease.

Elahere can cause severe ocular toxicity and its accelerated approval is contingent upon verification and description of clinical benefit in a confirmatory trial.

Elahere dosage is body weight and is administered every 3 weeks until disease progression or unacceptable toxicity. ImmunoGen priced Elahere at $6,220 per 20 mg dose. Dosing is three – four vials per treatment cycle resulting in a cost of +- $18,500 — $25,000.

ImmunoGen did not disclose details related to distribution. The company did confirm that the target US patient base is only 5200.  Given this small patient opportunity it is likely that Elahere will be launched through specialty pharmacy distribution.

CLICK HERE to read the full press release

CLICK HERE to access prescribing information

Categories
Uncategorized

BioPlus Specialty Pharmacy Acquired by Elevance

One of the few 2022 specialty pharmacy acquisitions was announced recently.  Elevance Health will acquire long running BioPlus as it seeks to expand its specialty pharmacy services.  (BioPlus is one of the few mature Specialty Pharmacies that have not been acquired and taken out of the independent Specialty Pharmacy column.) Elevance is an insurer that was formerly known as Anthem Health…. BioPlus will be integrated into Elevance’s PBM, IngenioRx.

Elevance is continuing a trend of insurers scooping up SPs.  The deal was cut with Nautic Partners / CarepathRx which had invested in BioPlus some time ago. 

Looking back a bunch of years we found that there has been scant press about BioPlus (save a little faux pas related to a HIPAA violation earlier this year.) Also, BioPlus did not make the 2021, Top 15 Largest SP list….. so we don’t have any solid idea about revenues.

Why are insurers keen on integrating SPs into their portfolios?  

In a word, money….. and leverage (that’s two words). A well-run SP…. with enough volume will be profitable. Elevance can steer plan members into their PBM, IngenioRx, and thereby to there specialty pharmacy. That supercharges profit opportunity. And, PBMs love leverage over manufacturers. Being able to put large specialty purchases on the table goes a long way in negotiations for rebates, etc.

Financial terms of the deal were not disclosed.

———————————————————————

Elevance Health to Acquire BioPlus

Acquisition deepens Elevance Health’s capabilities in specialty pharmacy

November 09, 2022 

INDIANAPOLIS–(BUSINESS WIRE)–Elevance Health (NYSE: ELV) today announced that it has entered into an agreement with CarepathRx, a portfolio company of Nautic Partners, to acquire BioPlus, a comprehensive specialty pharmacy. BioPlus provides a complete range of specialty pharmacy services for patients living with complex and chronic conditions, such as cancer, multiple sclerosis, hepatitis C, autoimmune diseases, and rheumatology. This acquisition will help Elevance Health meet the specialty drug needs of its clients and customers with a whole-health approach, supported by integrated programs across Elevance Health and Carelon, Elevance Health’s healthcare services brand.

“In making BioPlus part of the Elevance Health family, we are committed to leveraging our resources to scale and broaden the reach of BioPlus’ best-in-class specialty pharmacy capabilities, delivering greater affordability and access to critical medications.”

Tweet this

“As a trusted, lifetime health partner, the acquisition of BioPlus helps us deliver on our whole-health strategy that gives our consumers improved access and reliability to their prescriptions when they need it most,” said Pete Haytaian, Executive Vice President, Elevance Health and President, Carelon. “In making BioPlus part of the Elevance Health family, we are committed to leveraging our resources to scale and broaden the reach of BioPlus’ best-in-class specialty pharmacy capabilities, delivering greater affordability and access to critical medications.”

The company will look to expand BioPlus’ speed and service models across more complex disease treatment areas to provide timely access to medication, deliver leading support services for both providers and patients, and ensure individuals receive distinctive clinical expertise and service at all levels of care.

BioPlus currently offers Centers of Excellence (CoEs), which address therapeutic areas such as oncology and multiple sclerosis, and Elevance Health will look to build out additional CoEs for therapeutic areas to serve consumers. CoEs include teams of specialized pharmacists and clinicians knowledgeable in therapeutics areas who partner with patients throughout their treatment journey. These services help ensure medication access, adherence, and high-quality health outcomes.

After the acquisition closes, the specialty pharmacy will operate as part of IngenioRx, Elevance Health’s pharmacy benefit manager within Carelon, Elevance Health’s healthcare services brand. BioPlus’ offerings will complement IngenioRx capabilities and will increase Elevance Health’s ability to provide end-to-end pharmacy services, act as a patient advocate for integrated services, and promote affordability.

After BioPlus is integrated into Elevance Health, consumers who receive both medical and pharmacy benefits from Elevance Health’s subsidiaries will benefit from the company’s ability to leverage medical and pharmacy data to deliver proactive, whole-health insights. Carelon will connect its businesses through its digital platform, so in situations where BioPlus’ pharmacy team identifies a patient who may need behavioral health support or in-home care services, that team will be able to seamlessly connect that patient to services to address their whole health needs.

The acquisition is subject to customary closing conditions and is expected to close in the first half of 2023. BioPlus is not expected to have a material impact on adjusted earnings per share in 2023.

About Elevance Health, Inc.

Elevance Health is a lifetime, trusted health partner fueled by its purpose to improve the health of humanity. The company supports consumers, families, and communities across the entire care journey – connecting them to the care, support, and resources they need to lead healthier lives. Elevance Health’s companies serve more than 119 million people through a diverse portfolio of industry-leading medical, digital, pharmacy, behavioral, clinical, and complex care solutions. For more information, please visit www.elevancehealth.com or follow us @ElevanceHealth on Twitter and Elevance Health on LinkedIn.

About CarepathRx

CarepathRx seeks to transform pharmacy care delivery for health systems and hospitals by delivering improved patient outcomes that drive clinical, quality, and financial results. Through an industry leading, comprehensive, end-to-end hospital pharmacy care delivery model, CarepathRx works to turn hospital pharmacy into an active care management strategy and revenue generator while providing support across the patient’s complete healthcare journey. The company takes an enterprise approach, providing a powerful combination of technology, market-leading clinical pharmacy services, and wrap-around services that aim to optimize pharmacy performance for fully integrated pharmacy operations, expanded healthcare services, improved ambulatory access, minimized clinical variation, and new health system revenue streams. Today, CarepathRx serves more than 20 health systems and 600 hospitals, with more than 2,000 employees nationwide. For more information about CarepathRx, visit www.carepathrxllc.com.

About Nautic

Nautic Partners, LLC (“Nautic”) is a middle-market private equity firm that focuses on three industries: healthcare, industrials, and services. Nautic has completed over 150 platform transactions throughout its 35-plus year history. Nautic’s strategy is to partner with management teams to accelerate the growth trajectory of its portfolio companies via add-on acquisitions, targeted operating initiatives, and increased management team depth. For more information, please visit www.nautic.com.

Categories
Uncategorized

Look Back at Medicare Drug Price Legislation Efforts

There is a general understanding that Big Pharma spent a lot of effort and $$$s to counter-detail legislation to allow price negotiations in Medicare. They viewed any move in that direction as a red line thinking that any crack in the dam would evolve to potentially include all federal drug purchases. 

The article below offers a good look back of those efforts. It lays out the depths to which Big Pharma went to defend their long-held strangle hold on prices. Few know that PhRMA spent over $100 million this year to unleash a massive army of 1,500 lobbyists on Capitol Hill.

Pharma’s battle cry went for the heartstrings of Americans….. federal price negotiations will “immediately halt private funding of drug discovery and development”…. a “tragic loss for patients.” That’s a voter attention getter.

What Pharma hoped would get lost in the noise is that the Congressional Budget Office estimated Medicare would realize savings of $102 billion over 10 years. To get past the finish line, the legislation was watered down to start in 2026 with only 10 drugs. 

Price negotiation will face ongoing withering attacks and Pharma will not rest. A new congress will be lobbied starting on day one to stall or even reverse the modest progress to date. 

——————————————————————————————–

Big pharma went all in to kill drug pricing negotiations

For decades, the drug industry has yelled bloody murder each time Congress considered a regulatory measure that threatened its profits. But the hyperbole reached a new pitch in [2022] to adopt modest drug pricing negotiation measures in the Inflation Reduction Act.

The bill “could propel us light-years back into the dark ages of biomedical research,” Dr. Michelle McMurry-Heath, president of the Biotechnology Innovation Organization, said last month. Venture capitalists and other opponents of the bill said that it “immediately will halt private funding of drug discovery and development.”

Steve Ubl, leader of the ubiquitous Pharmaceutical Research and Manufacturers of America, or PhRMA, called the bill’s Senate passage a “tragic loss for patients.” He threatened in an interview with Politico to make politicians suffer if they voted for the measure, adding that “few associations have all the tools of modern political advocacy at their disposal in the way that PhRMA does.”

In the past 12 months, PhRMA and closely allied groups spent at least $57 million — $19 million of it since July — on TV, cable, radio, and social media ads opposing price negotiations, according to monitoring by the advocacy group Patients for Affordable Drugs. PhRMA spent over $100 million this year to unleash a massive team of 1,500 lobbyists on Capitol Hill.

The final bill is weaker than earlier versions, which would have extended negotiations to more drugs and included private insurance plans. The bill would enable only Medicare to negotiate prices beginning in 2026, initially for just 10 drugs.

It would save the Centers for Medicare & Medicaid Services about $102 billion over a decade, the Congressional Budget Office estimates. In 2021 alone, the top U.S. pharmaceutical companies booked tens of billions of dollars in revenue: Johnson & Johnson ($94 billion), Pfizer ($81 billion), AbbVie ($56 billion), Merck & Co. ($49 billion), and Bristol Myers Squibb ($46 billion).

The bill authorizes hundreds of millions of dollars for CMS to create a drug negotiation program, setting in motion a system of cost-benefit evaluations like those used in Europe to guide price negotiations with the industry. Americans pay, on average, four times what many Europeans do — and sometimes far, far more — for the same drugs.

The bill does not affect the list prices companies charge for new drugs, which increased from a median price of $2,115 in 2008 to a staggering $180,007 in 2021, according to recent research.

The bill’s champions say that PhRMA’s gloomy prophecies are overblown, and that history is on their side.

“It’s complete bullshit and a scare tactic,” Andy Slavitt told KHN. As a leading federal health official in 2016, he tried to change part of a Medicare program that pays doctors a fixed 6% of the cost of a drug each time they administer it, creating an incentive to use the most expensive infusion drugs. PhRMA funded most of the loud campaign that defeated his efforts, Slavitt said.

Another scare tactic: The drug industry warns that any price negotiation will kill innovation. Such warnings “constitute the pharma response in literally every instance since 1906,” the year the first drug regulation agency was created, said Dr. Aaron Kesselheim, who leads the Program on Regulation, Therapeutics, and Law at Brigham and Women’s Hospital in Boston. And yet, he said, regulatory changes rarely choked out investment in new drugs.

For example, the drug industry bemoaned a bill to boost generic drugs sponsored by Rep. Henry Waxman (D-Calif.) in 1984. Yet while 50% of prescribed drugs were generics in 2000 — up from 15% in 1980 — approvals of important new drugs also soared during the period, Kesselheim noted. The threat of losing market share to generics, he said, may have induced manufacturers to invest in innovation.

In 1993, Thomas Copmann, then a PhRMA vice president, charged that President Bill Clinton’s Vaccines for Children program, which funded vaccinations for any kid whose parents couldn’t afford them, “would just kill innovation because the government would control the market.” Over the next 16 years, childhood vaccination rates climbed — from 72% to around 93% for polio vaccine, for example. Over the same period, new vaccines against hepatitis A and B, pneumonia, chickenpox, human papillomavirus, and rotavirus were added to the schedule.

The drug industry’s attacks on regulation have a rich and florid history. In the early 1900s, the Proprietary Association of America warned newspapers that their advertising revenue would dry up if the industry had to list its ingredients (mostly alcohol). The law passed in 1906, but newspapers — and the drug industry — survived it.

Sometimes the industry’s breast-beating is a negotiating tactic, one that has led to concessions from Congress and the federal government.

In the 1990s, when discussions began about requiring drug companies to pay user fees to have their drugs reviewed, the industry described the fees as a “tax on innovation.” Eventually, it agreed to pay the fees if the FDA set deadlines for the reviews. The resulting boost in FDA staffing levels ushered in an increase in drug approvals over the ensuing five years.

Yet “killing innovation” remains a go-to trope. Drug imports, efforts to rein in “pay-for-delay” agreements between brand and generic companies, investigations of price gouging by drugmakers — all, according to conservatives and pharmaceutical executives, “kill innovation.” Former House Speaker Newt Gingrich in 2009 said the same about the Affordable Care Act. A golden decade for new drugs followed, with FDA approvals increasing from 21 in 2010 to 50 in 2021.

Critics of the bill argued that history and economic research show that drug investment will lag when markets shrink, which they say will be the case if price controls lead corporations to earn less money on their blockbuster drugs.

If Medicare negotiations cut into the profits of the biggest earners, investors in risky biotech companies, whose drugs rarely strike it rich, will shift some of their portfolios from pharmaceuticals into other sectors, said Craig Garthwaite, director of health care at Northwestern University’s Kellogg School of Management. “There’s a fair argument as to how much,” he said.

He noted that after Medicare’s drug program was created in 2003 — the drug industry initially opposed it — an increase in federal spending on medicines inspired pharmaceutical companies to spend more on drugs aimed at older people. “Once you invest in clinical trials, that money never comes back unless it’s in revenue for products sold,” he said.

The moribund antibiotics industry demonstrates how shrinking markets — hospitals and doctors intentionally limit the use of new drugs to reduce microbial resistance — lead to lower investment, Garthwaite said.

Yet some experts argue that Medicare drug pricing negotiations could hasten innovation if they steer companies away from drugs that modestly improve outcomes but can earn massive amounts of cash in the current system of unchecked prices.

In the cancer field, most investment is in drugs that provide incremental benefits at a high price, said Dr. Vincent Rajkumar, a Mayo Clinic oncologist. He was a principal investigator on two large trials testing Ninlaro (ixazomib), a pill for multiple myeloma that is very similar to the injected drug Velcade (bortezomib). While more convenient, Ninlaro is no more effective, he said, and it costs about eight times as much as generic bortezomib. A newer multiple myeloma drug, Xpovio (selinexor), keeps patients progression-free for about four additional months; it costs $22,000 a month.

Most new cancer drugs extend life for only a short time, said Rajkumar, who helped organize a 2015 letter signed by 118 oncologists that called for giving Medicare the power to bargain. If forced to negotiate, “maybe the companies would spend their research and development funds on something more meaningful,” he said.

In other high-income countries, drug price negotiations are the norm. “Right now, we are the odd man out,” Rajkumar said. “Are we really that brainy that we are right and everyone else is wrong? Are we really looking out for our public better than everyone else?”

Large patient groups such as the American Cancer Society, American Heart Association, and American Diabetes Association, all of which have significant drug industry support, stayed on the sidelines of the debate over the language in the drug price negotiation bill.

Some other patient groups, fearful that the industry will lose interest in drugs for smaller populations should prices decline, opposed the bill — and successfully won exceptions that would prevent Medicare from negotiating prices on drugs for rare diseases.

David Mitchell, a multiple myeloma patient who founded Patients for Affordable Drugs in 2017, said he’s sure the bill won’t discourage innovation — and his life may depend on it. The 68-year-old said he’s on a four-drug regimen but “cancer is very clever and finds a way to get around drugs.”

“The idea that taking a small bite out of pharma revenue is going to stop them from creating new drugs is bullshit,” he said.

Kaiser Health News: This article was reprinted from khn.org with permission from the Henry J. Kaiser Family Foundation. Kaiser Health News, an editorially independent news service, is a program of the Kaiser Family Foundation, a nonpartisan health care policy research organization unaffiliated with Kaiser Permanente.

Reviewed by Emily Henderson, B.Sc.

CLICK HERE to access this article

Categories
Uncategorized

Clearway Health to Open Hospital-Owned Specialty Pharmacies

We’ve often written about companies that work with hospitals to develop owned-and-operated specialty pharmacies. Those pharmacies boast that they that are significantly better than independent specialty pharmacies and they deserve to keep the prescriptions that their doctors write. Such companies include Shields Health (which acquired competitor ExceleraRx now part of Walgreens) as well as TrellisRx (acquired by CPS Solutions).

The valuation of these acquired companies were astronomical and that kind of $opportunity$ attracts even more competition. Some weeks ago, Cornerstone Health Solutions, which builds ‘specialty pharmacy accelerator programs’ for hospitals and health systems, announced that they are going head-to-head with Shields and CPS. They rebranded the company Clearway Health.  Name aside, it portends more competition for independent specialty pharmacies as health systems rush to open their own specialty pharmacies.

It is noteworthy that the genesis of Clearway Health is Bahston Medical Center Health Systems….. oops, Boston. It is unique that a hospital system has started a dedicated business targeting the creation of specialty pharmacies for other hospitals . Their press release said, “Clearway Health joins with hospitals and health systems to improve access to care and manage the complex medication needs of patient populations – strengthening the patient experience and driving revenue for clients.”

Time will tell if Clearway Health will be a better mousetrap.

CLICK HERE for more information

This website uses cookies to ensure you get the best experience on our website.