Albert Bourla (Evan Vucci, AP Images)
After a post-marketing trial for Pfizer’s Xeljanz turned concerning safety results at the beginning of the year, thwarting the whole JAK class, the FDA is finally rolling out some new approvals — but with added warnings and a key label change.
Both Xeljanz and AbbVie’s Rinvoq got cleared for new indications on Tuesday, but on one condition: They can only be taken after a patient has failed on one or more tumor necrosis factor (TNF) blockers, like Humira or Enbrel.
Earlier this month, the FDA slapped boxed warnings on the labels of Xeljanz, Rinvoq and Eli Lilly’s Olumiant, flagging the risk of cardiovascular events such as heart attack or stroke in high-risk patients who are 50 years and older, especially those with other risk factors such as current or past smokers.
Xeljanz is now approved for adults with active ankylosing spondylitis, a rare type of arthritis that causes pain and stiffness in the spine. And Rinvoq pulled a win in adults with active psoriatic arthritis, a type of inflammatory arthritis that causes joint pain, stiffness and swelling.
The latest fallout over JAK safety began back in January, when Xeljanz failed a six-year post-marketing safety study across 4,362 rheumatoid arthritis patients. Researchers found that those who received either a low or high dose of Xeljanz experienced more major cardiovascular events — such as stroke and heart attack — than those on Humira or Enbrel. They also had higher rates of cancer, with Pfizer failing to hit non-inferiority on both primary endpoints.
The study renewed some difficult questions for JAK inhibitors more broadly, a class that generated significant efficacy in autoimmune conditions but faced repeated safety concerns.
In the first week of December, the FDA concluded that there’s an increased risk of serious heart-related events such as heart attack or stroke, cancer, blood clots and death associated with Xeljanz, and put updated warnings on that drug and two others. Although Olumiant and Rinvoq hadn’t been studied in large safety trials, regulators decided that they may pose similar risks, as they share the same mechanism of action.
Investors were muted on the news of AbbVie and Pfizer’s new approvals, with the company’s stock, $ABBV and $PFE, up about 1% in pre-market trading on Tuesday.
The Xeljanz approval is based on data from a Phase III trial, showing that twice-daily 5 mg doses of the blockbuster drug helped 56.4% of patients achieve an improvement of at least 20% on the Assessment in SpondyloArthritis international Society scale (ASAS20), compared to just 29.4% of placebo patients (p<0.0001).
Just over 40% of patients on Xeljanz achieved an ASAS40 response, compared to 12.5% on placebo, according to Pfizer. The safety profile was similar to that in approved indications of rheumatoid arthritis and psoriatic arthritis, the company said.
Meanwhile, Rinvoq helped psoriatic arthritis patients treated with 15 mg doses achieve higher ACR50 responses (an improvement of at least 50% on the American College of Rheumatology scale) compared to placebo in two Phase III trials. In the trials, 38% and 32% of patients on Rinvoq achieved ACR50, compared to 13% and 5% on placebo, respectively.
The Rinvoq arms also boasted 16% and 9% ACR70 responses, compared to 2% and 1% in the placebo arms, respectively. And the drug was seen to significantly inhibit the progression of structural joint damage compared to placebo, according to AbbVie. The company said Rinvoq’s safety profile was consistent with that in patients with rheumatoid arthritis.
Now, we’ll wait to see if the added warnings affect the drugs’ performances. Xeljanz pulled in $2.4 billion in 2020, and Rinvoq was a bit behind it with $731 million in net sales.
Sensor-based technology for clinical trial data collection represents the latest medical paradigm shift. There are more than 700 clinical studies involving wearable devices currently underway in the United States. A study from Intel IT projects their inclusion in clinical trials will surge to 70% by 2025.
Apps, biosensors and patient-centered technologies increase visibility of comprehensive patient data. Pharma leaders anticipate the benefits of wearables to include better data (58%), faster results (33%) and lower trial costs (10%).
A nurse administers a COVID-19 booster shot to Joe Rigdon at a vaccination site in Eastmonte Park, Altamonte Springs. (Photo by Paul Hennessy/SOPA Images/LightRocket via Getty Images)
When Laura Burns went to get her first Covid-19 shot last January, no one had warned her that the vaccines might not work for her.
Burns, the recipient of a double-lung transplant in 2016, knew to be careful about the medicines she took. She consulted with her transplant team when the Pfizer and Moderna shots were authorized and only signed up after being told the vaccines would likely be safe for her, which they were.
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Jay Bradner, President, Novartis Institutes for BioMedical Research
John Carroll: Well, hello everybody. This is John Carroll. I’m the editor of Endpoints News, the editor and founder of Endpoints News. I’m here with Jay Bradner, the president of the Novartis Institutes for BioMedical Research. Jay, we’re going to be talking about ASH in just a second, but you’ve just recently celebrated your sixth anniversary as president of NIBR. And I’m curious, it’s such a significant amount of time for anybody to spend in one career phase. And looking back over the last six years, is everything fundamentally different about the research process and the translational arena that you’re in?
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We will now have to wait until 2022 to find out whether Sanofi and GlaxoSmithKline have an effective recombinant vaccine against Covid-19.
The two pharma giants revealed that their Phase III trial isn’t quite ready for a readout. Meanwhile, they seem to have more hope in the booster application of their candidate, touting positive preliminary data suggesting that it spurred an increase in neutralizing antibodies in all patients — whether they received mRNA or adenovirus-based shots as the primary vaccines.
Harpreet Singh, Immatics CEO (Credit: Allogeneic Cell Therapies Summit)
Just a few weeks after offering a positive readout on its first early clinical-stage offering, the transatlantic biotech Immatics is back with news that the research crowd around Rupert Vessey at Bristol Myers Squibb has anted up $150 million in cash to get on at the ground floor with one of their still-preclinical efforts.
This time the news is centered on IMA401, Immatics’ most advanced bispecific, which uses one binder to latch on to MAGEA4/8 while another is used to whip up T cell activity against tumor cells where that’s a common antigen. For now, that’s still a preclinical effort, with the first human trial set to launch in the first half of next year.
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Robert Califf (L) shakes hands with Sen. Mitt Romney (R-UT) at Califf’s confirmation hearing for FDA commissioner, Dec. 14, 2021 (Graeme Sloan/Sipa via AP Images)
Rob Califf, the famous cardiologist from Duke University, is likely to return to the top of the FDA, this time under the Biden administration.
At his confirmation hearing Tuesday, Democrats and Republicans on the Senate health committee offered their support for Califf, with Chair Patty Murray (D-WA) stressing the need for an experienced leader, like Califf, who can ensure that science comes first.
Though it’s already publicly traded in the US and Hong Kong, BeiGene went and triple-listed itself in Shanghai’s stock exchange as well. But early returns have reportedly been far from promising.
BeiGene shares in Shanghai fell more than 16% after debuting Wednesday, following a $3.5 billion raise for the biotech. It had been the year’s biggest IPO on the Shanghai stock exchange, known as STAR, as well as the largest IPO offering by any Chinese healthcare firm in at least the last two decades, according to the report.
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Soon after San Francisco-based Genentech won an EUA for tocilizumab as a treatment for hospitalized Covid patients last summer, the company announced a shortage of the drug while pointing to the emergence of the Delta variant and the slowing of vaccination rates across the US.
‘This new wave of the pandemic has led to Genentech experiencing an unprecedented demand for Actemra IV– well-over 400% of pre-COVID levels over the last two weeks alone and it continues to increase,’ the company said in August.
CVS Health is adding clinical trial services inside some of its retail locations with HealthHubs and in the future at CVS primary care centers (via CVS Health)
During the Covid-19 pandemic, local pharmacies were not only key purveyors of prescriptions and hand sanitizer, but also important testing and vaccine delivery locations. Next up? Clinical trial sites. That’s according to a recent PwC Health report that lays out the case for both pharma and pharmacies — and why it’s more probable than ever.
Figuring out how to scale decentralized trials is necessary, made clear by the pandemic, said Greg Rotz, PwC’s pharma and life sciences leader in the US. The good news from his perspective is both pharma companies and retailers are investing in business models and infrastructure to make it happen.
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