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Monday, September 2, 2019

Community Health Workers Slinging Free Heart Drugs Cut Cardiovascular Risks

A tailored community-based intervention that leaned on the various skills of non-physician health workers (NPHWs) cut the risk of cardiovascular disease in patients with high blood pressure, results of the HOPE 4 trial showed.
Patients exposed to the intervention had an 11.17% reduction (-12.88 to -9.47) in Framingham Risk Score at 12 months versus a 6.40% reduction (95% CI -8.00 to -4.80) in the usual care group, reported Jon-David Schwalm, MD, MSc, of McMaster University and Hamilton Health Sciences in Hamilton, Ontario.
“A comprehensive model of care led by non-physician heath workers, involving primary care physicians and family, along with the provision of free antihypertensive medications and a statin, resulted in a greater than 40% reduction in cardiovascular risk and a doubling in the change in blood pressure control,” he said during a press briefing here at the 2019 European Society of Cardiology congress.
HOPE 4 was a cluster randomized trial in Colombia and Malaysia that used NPHWs to screen and treat participants. The NPHWs used tablets with guideline-recommended treatment algorithms to determine appropriate therapy (after training they attained 93% concordance with physicians) — patients received free antihypertensives and a statin. Family and community members served to support the study participants in terms of lifestyle changes and drug adherence.
In all, 69% of patients in the intervention group were able to get their blood pressure under control (systolic blood pressure [SBP] <140 mm Hg) compared with 30% in the usual care group (P<0.0001).
The intervention group’s 4.78% absolute reduction (95% CI -7.11 to -2.44) in ten-year predicted cardiovascular disease risk — the study’s primary outcome — was underpinned by greater reductions in SBP and LDL cholesterol (P<0.0001 for all):
  • SBP: 11.45 mm Hg (95% CI -14.94 to -7.97)
  • LDL: 0.41 mmol/L (95% CI -0.60 to -0.23)
No significant differences were seen for glucose concentrations or HDL. Results of the study were presented during a late-breaking trials session and published simultaneously in The Lancet.
The tailored aspect of the trial involved an initial systematic analysis of each country to identify patient-, provider-, and healthcare-system barriers to hypertension care. In Colombia for example, while blood pressure drugs may be subsidized for low-income individuals, long wait times often dissuade patients from bothering. In HOPE 4, locally available generic medications were made available free of charge for starters, and the NPHWs delivered them to patients’ homes in some cases.
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Jon-David Schwalm, MD, MSc, discussing the HOPE 4 results at ESC
These workers were already working in the communities and were “repurposed” for cardiovascular disease prevention. “It’s a matter of shifting direction,” Schwalm told MedPage Today.
Asked what lessons could be applied to North America, he said his group piloted the program in Canada, using firefighters as the NPHWs.
“In Canada, medication was not so much an issue,” he said. “Finding what are the barriers in individual countries, I think that’s where we are going to see the biggest benefit.”
Researchers are ever seeking innovative ways to get antihypertensive treatments to patients. At last year’s American College of Cardiology meeting, for example, a group from the University of California Los Angeles made a splash showing a 27 mm Hg drop in blood pressure when pharmacists at barbershops doled out antihypertensives (patients’ primary care physicians had signed off).
In a linked comment in The Lancet, Tazeen H. Jafar, MD, MPH, of Duke-NUS Medical School in Singapore, and colleagues noted that the large effect size observed in the trial, compared with other pragmatic studies, can likely be explained by several key factors.
For starters, patients in HOPE 4 were high risk at baseline (mean Framingham Risk Score >30%). Second, the study relied on NPHWs who possess a “higher mix of skills and competencies,” which is not always the case in such trials. Third, the trial opted for a free statin plus single-pill blood-pressure medication. Lastly, the use of patient support led to excellent adherence to the protocol (64% vs 40% in the usual care group).
“However, these same study design attributes might also limit sustainability and scalability. Of paramount importance is the concept of integration within the existing health-care system,” Jafar’s group wrote. “NPHWs in HOPE 4 were private contractors and hired exclusively for the trial. If staff were employees in existing health systems, rather than private contractors, competing tasks might compromise the acceptability, fidelity, effectiveness, and sustainability of the HOPE 4 intervention strategies when scaled up in the real world.”
They called for a comprehensive analysis to determine the cost-effectiveness of such an approach; Schwalm said his group is in the process of working on such an analysis.
“HOPE 4 and similar highly important studies should prompt the scientific and legislative communities to rethink the scale-up of large, evidence-based approaches to dramatically reduce the burden of uncontrolled hypertension and lower cardiovascular risk,” Jafar and coauthors wrote. “Such bold strategies cannot be ignored.”
From 2014 to 2017, the study enrolled 1,371 hypertensive patients age 50 and older who were screened from 30 communities in Colombia and Malaysia. Door-to-door hypertension screening was performed in Colombia while individuals in Malaysia were screened mostly at community gatherings. In all, 14 of these communities were randomized to the intervention while 16 received usual care.
HOPE 4 was funded by the Canadian Institutes of Health Research, Grand Challenges Canada, the Ontario SPOR Support Unit, the Ontario Ministry of Health and Long-Term Care, Boehringer Ingelheim, the World Health Organization, and the Population Health Research Institute.
Schwalm and co-authors disclosed institutional relationships with the study backers.
Jafar and co-authors declared no conflicts of interests.

Ardelyx Call Sept 3 to Review Results from Pivotal Phase 3 AMPLIFY Study

Ardelyx, Inc. (NASDAQ: ARDX), a specialized biopharmaceutical company focused on developing first-in-class medicines to improve treatment for people with cardiorenal diseases, announced that it will hold a conference call tomorrow, September 3, at 8:30 am Eastern Time to review the results from the pivotal Phase 3 AMPLIFY study of tenapanor in combination with phosphate binders in patients with chronic kidney disease on dialysis whose hyperphosphatemia was not controlled with binders. Tenapanor is Ardelyx’s investigational, first-in-class, small molecule, non-binder, phosphate absorption inhibitor.
To participate in the conference call, please dial (855) 296-9612 (domestic) or (920) 663-6277 (international) and refer to conference ID 9789472. Live audio of the conference call will be simultaneously webcast and will be available under the Investors section of the company’s website at www.ardelyx.com. The webcast will be archived and available for replay for 60 days following the call.

HealthEquity Q2 2020 Earnings Preview

HealthEquity (NASDAQ:HQY) is scheduled to announce Q2 earnings results on Tuesday, September 3rd, after market close.
The consensus EPS Estimate is $0.35 (+2.9% Y/Y) and the consensus Revenue Estimate is $85.28M (+20.0% Y/Y).
Over the last 2 years, HQY has beaten EPS estimates 88% of the time and has beaten revenue estimates 100% of the time.
Over the last 3 months, EPS estimates have seen 2 upward revisions and 4 downward. Revenue estimates have seen 6 upward revisions and 0 downward.

Lilly’s generic insulin not widely used yet

While Eli Lilly’s generic insulin has been approved since March, a significant portion of prescription claims are still for its brand-name counterpart, Humalog, according to an analysis from drug price tracker GoodRx.
Generic insulin lispro’s list price is more than 65 percent cheaper than Humalog at $265 for a pack of five pens. Still, GoodRx found only 8 percent of prescription fills are for generic insulin lispro, while the majority are still for Humalog.
“This low fill count is likely a result of shortages of the medication in certain areas and spotty insurance coverage,” according to GoodRx.
Comparatively, drugmaker Sanofi recently lowered the price of its insulin drug Admelog by 46 percent. It is now more affordable than even generic Humalog.
Read more here.

ESC: Most cardio events avoidable with small blood pressure, cholesterol cuts

The majority of heart attacks, strokes, and deaths from heart disease can be prevented with modest and sustained decreases in blood pressure and cholesterol. The late breaking results are presented in a Hot Line Session today at ESC Congress 2019 together with the World Congress of Cardiology(1) and published in the Journal of the American Medical Association.(2)
Principal investigator Professor Brian Ference of the University of Cambridge, UK said: “Healthy eating and physical activity are effective ways to improve cardiovascular health. The best diet or exercise programme differs for each person. It is the one that produces the greatest reductions in both blood pressure and cholesterol for that person AND to which he or she can adhere because the benefits of the reductions accrue overtime.”
The study found that long-term exposure to the combination of both lower low-density lipoprotein cholesterol (LDL-C) and lower systolic blood pressure (SBP) was linked with independent and additive reductions in the lifetime risk of cardiovascular disease.
The relationship was dose-dependent, meaning that any combination of lower LDL-C and lower SBP was associated with a corresponding reduction in lifetime risk.
The study shows that even small declines in LDL-C and SBP can substantially diminish the likelihood of ever having a heart attack or stroke. For example, the combination of 0.3 mmol/L (14 mg/dL) lower LDL-C and 5 mmHg lower SBP was associated with a 50% lower lifetime risk of cardiovascular disease.
Prof Ference said: “These small modifications in LDL-C and SBP are the kind of changes that can be achieved by eating healthily such as the DASH diet3 or similar diets.”
Larger reductions in LDL-C and SBP with more aggressive lifestyle changes or other therapies to achieve the combination of 1 mmol/L (38.67 mg/dL) lower LDL-C and 10 mmHg lower SBP can reduce lifetime risk of cardiovascular disease by 80% and reduce lifetime risk of cardiovascular death by more than two-thirds (68%).
The study included 438,952 participants of the UK Biobank who experienced a total of 24,980 major coronary events (defined as the first occurrence of non-fatal heart attack, ischaemic stroke, or coronary death).  The average age was 65.2 years (range: 40.4 to 80.0) and 54% were female.
The researchers used genetic variants linked with lower LDL-C and SBP as instruments to randomly divide participants into groups with lifetime exposure to lower LDL-C, lower SBP, or both as compared to a reference group using a 2×2 factorial design. They then compared the differences in plasma LDL-C, SBP and cardiovascular event rates between the groups to estimate associations with lifetime risk of cardiovascular disease.
Prof Ference said: “It is important to encourage patients and populations to invest in their future health.  Maintaining even small reductions in both LDL-C and SBP for prolonged periods of time can pay very big health dividends by dramatically reducing the lifetime risk of cardiovascular disease.”

ESC: Bypass surgery, coronary stenting yield comparable 10-year survival

Ten-year survival rates are similar for bypass surgery and coronary stenting with drug-eluting stents in randomised patients with de novo three-vessel and left main coronary artery disease, according to late breaking results from the SYNTAX Extended Survival study presented in a Hot Line Session today at ESC Congress 2019 together with the World Congress of Cardiology (1) and published in The Lancet. (2)
Prespecified subgroup analyses showed that surgery provided a survival benefit in patients with three-vessel disease and more complex coronary artery disease, while no treatment differences were found in patients with left main disease.
Ischaemic heart disease is the top cause of death globally. Percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) are options for patients requiring revascularisation. European guidelines advise discussing these patients in a multidisciplinary Heart Team. (3)
Individual randomised trials comparing PCI with drug-eluting stents and CABG have not shown a survival benefit for either therapy at mid-term follow-up (e.g. up to five years). The SYNTAX trial was the first large-scale multicentre, randomised study in patients with de novo three-vessel and left main coronary artery disease that underwent PCI with drug-eluting stents or CABG. When clinical equipoise between PCI and CABG was presumed by the Heart Team, 1,800 patients were randomly assigned to PCI with paclitaxel-eluting stents (n=903) or CABG (n=897). Survival curves started to diverge after one-year follow-up(4) and continued to diverge up to five years, but without reaching statistical significance. (5)
The SYNTAX Extended Survival (SYNTAXES) study examined 10-year all-cause death rates in patients with de novo three-vessel and left main coronary artery disease randomised to PCI with drug-eluting stents or CABG in the SYNTAX trial. All 85 SYNTAX sites from 18 North American and European countries were contacted to provide survival data, which was obtained from healthcare records and national death registries. Completeness of follow-up was achieved in 94% of patients and was well-balanced between the CABG and PCI arms.
At 10-year follow-up, there was no survival difference between PCI with drug-eluting stents and CABG in the overall cohort of patients. There were 244 deaths after PCI and 211 after CABG (hazard ratio [HR] 1.17; 95% confidence interval [CI] 0.97–1.41; p=0.092).
When analyses were conducted according to prespecified subgroups, CABG provided a 10-year survival benefit over PCI in patients with three-vessel disease (151 deaths after PCI versus 113 after CABG; HR 1.41; 95% CI 1.10–1.80; p=0.006). CABG also provided a survival benefit in patients with increasingly complex coronary artery disease (defined by higher SYNTAX scores) – this was observed in the overall cohort and in those with three-vessel disease. In the subgroup of patients with left main coronary artery disease, no survival differences existed between PCI and CABG (93 patients died after PCI versus 98 after CABG; HR 0.90; 95% CI 0.68–1.20; p=0.47). This resulted in a treatment-by-subgroup interaction according to the presence or absence of left main coronary artery disease (p for interaction=0.019). Furthermore, CABG and PCI resulted in comparable 10-year survival in patients with and without diabetes.
First author Dr Daniel Thuijs of the Erasmus University Medical Centre, Rotterdam, the Netherlands said: “The SYNTAX Extended Survival study presents robust, clinically relevant, and complete 10-year randomised survival data and can aid a multidisciplinary Heart Team discussion in the process of deciding on the optimal treatment strategy for a patient with coronary artery disease requiring revascularisation.”

Biotech week ahead, Sept. 3

The biotech space saw muted activity in the week ended Aug. 30. Among the notable news of the week: Amgen, Inc. AMGN 0.79%‘s $13.4-billion deal to buy the psoriasis drug Otezla from Celgene Corporation CELG 0.32% and Johnson & Johnson JNJ 0.11%‘s $572-million settlement agreement with the state of Oklahoma in an opioid lawsuit.

Plus Therapeutics Inc PSTV 8.74%, which previously went by the name Cytori, was among the top performers in the biotech space, advancing in excess of 200% — with no clear catalyst driving the rally.
The following are key catalysts for biotech investors to watch in the unfolding week.

Conferences

  • European Society of Cardiology, or ESC, Congress 2019: Aug. 30-Sept. 4 in Paris, France.
  • Society for the Study of Inborn Errors of Metabolism, or SSIEM, Annual Symposium 2019: Sept. 3-6 in Amsterdam, Netherlands.
  • International Meeting on Dermatopathology & Skin Care: Sept. 4-5 in Paris.
  • Citi 14th Annual Biotech Conference: Sept. 4-5 in Boston, Massachusetts.
  • 2019 Wells Fargo Healthcare Conference: Sept. 4-5 in Boston.
  • Baird’s 2019 Global Healthcare Conference: Sept. 4-5 in New York City.
  • 4th International Congress on Addictive Behavior and Dual Diagnosis: Sept. 5-6 in Budapest, Hungary.
  • International Association for the Study of Lung Cancer, or IASLC, 2019 World Conference: Sept. 7-10 in Barcelona, Spain.

PDUFA Dates

The FDA is set to rule on Roche Holdings AG Basel ADR RHHBY 0.18%‘s Tecentriq along with chemotherapy as first-line treatment of metastatic non-squamous non-small cell lung cancer in patients who do not have EGFR or ALK genomic tumor aberrations. The PDUFA date is set for Monday, Sept. 2.

Clinical Trial Readouts

ESC Congress Presentations
AstraZeneca plc AZN 0.91%: already released Phase 3 data for Farxiga in heart failure as well as already released Phase 3 data for Brilinta in Type 2 diabetes (both scheduled for Sept. 1).
PhaseBio Pharmaceuticals Inc PHAS 2.92%: Phase 1 data for PB2452 as a reversal agent for AstraZeneca’s ticagrelor.
Alnylam Pharmaceuticals, Inc. ALNY 2.06% and The Medicines Company MDCO 2.4%: already released Phase 3 data for inclisiran that is being evaluated in a Phase 3 trial dubbed ORION 10 for atherosclerotic cardiovascular disease (Sept. 2).
SSIEM Annual Symposium Presentations
Aeglea Bio Therapeutics Inc AGLE 1.5%: Phase 1/2, 20-week repeat dose data for pegzilarginase in arginase 1 deficiency (Sept. 3).
Orchard Therapeutics PLC – ADR ORTX 2.99%: Phase 2 data for OTL-200 in metachromatic leukodystrophy (Sept. 4).
Synlogic Inc SYBX 6.69%: Full Phase 2 data for SYNB1619 in phenylketonuria (Sept. 4).
Mid-2019 Readouts
AnaptysBio Inc ANAB 1.65%: Phase 2 data for ANB019 in generalized pustular psoriasis.
Akcea Therapeutics Inc AKCA 0.99% and Ionis Pharmaceuticals Inc IONS 1.39%: Phase 2 pilot study data for AKCEA-ANGPTL3-LRx in rare hyperlipidemias.

Earnings

Tuesday
Zai Lab Ltd ZLAB 1.3%
Thursday
PAVmed Inc PAVM 1.06%