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Saturday, June 8, 2019

Biotech week ahead, June 10

Biotech stocks staged a steady recovery last week. ASCO presentations dominated the headlines, with Iovance Biotherapeutics Inc IOVA 3.36% and Mirati Therapeutics Inc MRTX 2.94% among the biggest gainers. The IPO calendar was empty and there were a slew of clinical trial readouts that swayed stocks.
The following are key catalysts expected in the unfolding week.

Conferences

  • American Diabetes Association 79th Scientific Sessions: June 7-11 in San Francisco, California.
  • 24th World Congress of Dermatology: June 10-15 in Milan, Italy.
  • Goldman Sachs 40th Annual Global Healthcare Conference: June 11-13 in Rancho Palos Verdes, California.
  • The Annual European Congress of Rheumatology of the European League Against Rheumatism: June 12-16 in Switzerland.
  • 24th European Hematology Association Congress: June 13-16 in Amsterdam, Netherlands.

PDUFA Dates

Merck & Co., Inc. MRK 1.14% awaits the FDA’s ruling on its sBLA for Keytruda as a first-line treatment option for patients with recurrent or metastatic head and neck squamous cell carcinoma. The PDUFA date is set for June 10.

Clinical Trial Readouts

American Diabetes Association 79th Scientific Sessions Presentations

NGM Biopharmaceuticals Inc NGM 3.09%: updated Phase 1b data for NGM313/MK-3655 (NASH and Type 2 diabetes)on June 9.

EULAR Annual European Congress Of Rheumatology Presentations

GALAPAGOS NV/S ADR GLPG 3.77% and Gilead Sciences, Inc. GILD 2.56%: already-released Phase 3 data for Filgotinib from FINCH 1 study (rheumatoid arthritis), June 12; Phase 3 data for Filgotinib from FINCH 3 study (rheumatoid arthritis), June 15.
Nektar Therapeutics NKTR 0.06%: Phase 1b data for NKTR-358 (systemic lupus erythematosus), June 13.
Corbus Pharmaceuticals Holdings Inc CRBP 3.41%: Phase 2 open-label data for Lenabasum (dermatomyositis), June 14; Phase 2 open-label data for Lenabasum (systemic sclerosis).
Kezar Life Sciences Inc KZR 3.91%: already-released initial Phase 1b topline data for KZR-616 (lupus), June 14.

24th European Hematology Association Congress Presentations

Kura Oncology Inc KURA 4.85%: Additional Phase 2 data for Tipifarnib (relapsed or refractory peripheral T-cell lymphoma), June 13.
bluebird bio Inc BLUE 3.79%: Phase 3 data for LentiGlobin in HGB-212 (transfusion-dependent beta thalassemia), June 14; updated Phase 1/2 data for LentiGlobin in HGB-204 (beta-thalassemia), June 14; updated Phase 3 data for LentiGlobin in HGB-207 (non-β0/β0 transfusion-dependent thalassemia), June 14.
Beigene Ltd BGNE 2.32%: updated Phase 1 data for Zanubrutinib (Waldenström’s macroglobulinemia), June 14; Phase 2 data for Tislelizumab (relapsed or refractory classical Hodgkin lymphoma), June 14.
Global Blood Therapeutics Inc GBT 1.15%: Phase 3 data for GBT440 (sickle cell disease), June 14.
Blueprint Medicines Corp BPMC 2.13%: updated Phase 1 data for Avapritinib BLU-285 (advanced Systemic mastocytosis), June 14.
ArQule, Inc. ARQL 2.04%: Phase 1a data for ARQ 531 (B-cell malignancies), June 14.
Regeneron Pharmaceuticals Inc REGN 2.38%: updated Phase 1 data for REGN1979 (non-Hodgkin lymphoma).
Sunesis Pharmaceuticals, Inc. SNSS 1.73%: updated Phase 1/2 data for SNS-062 ( advanced B-cell malignancies).
Sutro Biopharma Inc STRO 1.1%: Phase 1 initial safety data for STRO-001 (non-Hodgkin lymphoma), June 15.
Forty Seven Inc FTSV 3.11%: Phase 2 data for 5F9 + rituximab (non-Hodgkin lymphoma), June 15.
Geron Corporation GERN 2.9% : updated Phase 2 data for Imetelstat (Myelodysplastic syndromes), June 15.

24th World Congress of Dermatology Presentations

Incyte Corporation INCY 1.23%: Phase 2 data for ruxolitinib (atopic dermatitis), June 14; Phase 2 data for ruxolitinib (vitiligo), June 15

Weight Loss and Delays to Progression of Type 2 Diabetes

In a comparison of two different diet and two different weight management programs, results of the international PREVIEW intervention study found a low, similar rate of progression to type 2 diabetes (T2D) among people with prediabetes who had initially lost weight on a low-calorie diet (LCD), according to a symposium presentation today titled “PREVIEW Study Results—Prevention of Diabetes through Lifestyle Intervention and Population Studies Around the World” at the American Diabetes Association’s® (ADA’s) 79th Scientific Sessions® at the Moscone Convention Center in San Francisco. The study showed no difference between either of the post-weight loss diet or exercise-management programs, with the participants who had initially lost weight in all groups having a three-year incidence rate of T2D of 4%, which was much lower than anticipated.

In order to identify the most effective lifestyle patterns for the prevention of T2D in a population of people who have prediabetes and are overweight, researchers around the globe began “PREVention of diabetes through lifestyle Intervention and populations studies in Europe and around the World” (PREVIEW). The study’s aim was to determine the effects and interactions of different types of diets and different exercise regimens on the development of new cases of T2D in patients with prediabetes.
“Further work is needed to explore the reasons for such successful prevention of type 2 diabetes, however, it is likely that the initial weight loss combined with thorough education and support in the components in either nutrition plan, in addition to a physical activity program, led to successful lifestyle changes and maintenance of at least some of the initial weight loss in most of the people completing the trial,” said one of the lead investigators Ian Macdonald, BSc, PhD, professor of metabolic physiology at the University of Nottingham. “The inclusion of an initial period of a low-calorie diet achieving significant weight loss, preceding a well-structured and effectively delivered weight maintenance program, may be a major feature of future diabetes prevention programs.”
PREVIEW is, to-date, the largest multi-national trial to address T2D prevention in adults with prediabetes through nutrition and exercise. The study began in 2013 and enrolled 2,223 participants using intervention centers in DenmarkFinland, the United Kingdomthe NetherlandsSpainBulgariaAustralia, and New Zealand. The 36-month intervention consisted of two phases: a two-month period of rapid weight reduction achieved using an LCD (800 kcal/day), followed by a 34-month randomized diet and exercise phase for weight loss maintenance consisting of four treatment arms. The impact of a high-protein, low-glycemic index (GI) vs. moderate protein, moderate-GI diet in combination with moderate or high-intensity physical activity on the incidence of T2D and the related clinical end-points were investigated.

Lilly’s tirzepatide demonstrates benefits in data at American Diabetes Assn

Results from several studies of Eli Lilly and Company’s (LLY) investigational dual GIP and GLP-1 receptor agonist (RA), tirzepatide, reinforce its potential in lowering A1C and body weight in people with type 2 diabetes. Early research results also support tirzepatide’s potential benefit in treating other metabolic conditions. The following findings were presented in oral and poster presentations at the American Diabetes Association’s® 79th Scientific Sessions® in San Francisco:
  • improvements in markers of beta cell function (how cells in the pancreas produce, store and release insulin) and insulin sensitivity (how cells in the body respond to insulin) that help explain efficacy;1
  • efficacy and improved tolerability with lower initial doses and smaller subsequent dose escalations;2
  • significant A1C and body weight reductions in Japanese people with type 2 diabetes after just eight weeks of treatment;3 and
  • improvements in markers of non-alcoholic steatohepatitis (NASH, liver inflammation and cell damage caused by liver fat) in people with type 2 diabetes.4
“These new tirzepatide data build upon the positive results seen in people with type 2 diabetes to date,” said Juan P. Frias, M.D., Medical Director and Principal Investigator, National Research Institute. “The results offer additional evidence of tirzepatide’s potential to meaningfully reduce A1C and body weight in people with type 2 diabetes and treat other metabolic conditions.”

Search launched for first patient proven spontaneously cured of Alzheimer’s

Has any Alzheimer’s disease (AD) patient ever been proven cured spontaneously of the usually fatal disease, without medical intervention? That’s what Alzheimer’s Germ Quest, Inc., wants to find out. They’re offering a $100,000 reward to the physician who provides the best case. Presently there is no curative for AD, and it is considered 100 percent fatal.

“Researchers can get valuable clues to a disease’s cause and possible therapy from studying even a single spontaneously-cured individual,” says Leslie Norins, M.D., Ph.D., the CEO. “We want to find such an unusual AD patient if one exists, and get the details for scientists to review. Speedier progress against Alzheimer’s is vital.”
“It might have been reported as a miracle. So, we contacted the authorities of the Catholic Church to see if they had records of any miraculous cures of AD,” Dr. Norins says.
The Catholic evaluator and registrar of miracles is the Congregation for the Causes of Saints, part of the Curia at the Holy See, in Rome. “Their letter to me says they know of none,” says Dr. Norins. We also got negative reports from the research librarians at Catholic University of America and the University of Notre Dame.
Next, Dr. Norins says he searched both the medical and lay literature, using both PubMed and Google, and again turned up no spontaneous cures of AD.
So, he says, “We’re creating our own dragnet through this global search. Because physicians are the local professionals best able to diagnose AD and assess a possible spontaneous cure, we are targeting them. We’re asking any doctor who has convincing evidence to submit that case via our website, ALZgerm.org, where they’ll find all the details.”
Dr. Norins cites as inspiration the single patient whose proven cancer spontaneously disappeared, leading Dr. Steven Rosenberg of the National Cancer Institute to begin his productive studies of immunological remedies for cancer. Other single-patient discoveries include the “Philadelphia chromosome” in leukemia, and the “Berlin patient” for white cell resistance to HIV.
Alzheimer’s Germ Quest, Inc. is a self-funded public benefit corporation headquartered in Naples, Florida. It sponsors the $1 Million Challenge Award for the scientist who provides persuasive evidence that AD is caused by an infectious agent.

Heart (and Kidneys) Feature in Diabetes Trials in San Francisco

Results from 10 major clinical trials addressing prevention and management of type 2 diabetes will be featured at the American Diabetes Association 2019 Scientific Sessions.
Spread across the 5-day meeting from Friday June 7 through Tuesday June 11, the 10 “highly anticipated study announcements of 2019” will include new cardiovascular outcomes trial (CVOT) results for dulaglutide (Trulicity, Lilly), linagliptin (Tradjenta, Lilly/Boehringer Ingelheim), dapagliflozin (Farxiga/Forxiga, AstraZeneca), and oral semaglutide (Ozempic, Novo Nordisk), and new cardiorenal data for canagliflozin (Invokana, Janssen) and linagliptin.
Other major study results address the roles of vitamin D, lifestyle modification, and medication use in type 2 diabetes prevention.
“The hottest clinical areas in diabetes have to do with the potential cardiovascular and renal outcomes for some of the newer agents, especially the sodium-glucose cotransporter type 2 [SGLT2] inhibitors and glucagon-like peptide 1 receptor [GLP-1] agonists. Particularly salient at this meeting will be several trials regarding these outcomes,” program chair Jose C. Florez, MD, PhD, professor of medicine at Harvard and chief of the endocrine division at Massachusetts General Hospital, Boston, told Medscape Medical News.
Florez said that the recent flow of new data showing cardiovascular and renal benefits for glucose-lowering drugs “is really exciting to see. I think it’s really shifting the algorithm for what agents people use in type 2 diabetes and in what sequence.”
“Some of these trials will have a major impact on how we” practice medicine, said ADA Science and Medicine President Louis H. Philipson, MD, PhD, director of the Kovler Diabetes Center, and James C. Tyree professor of diabetes research and care, Departments of Medicine and Pediatrics, University of Chicago, Illinois.
And not forgetting type 1 diabetes, there are eagerly awaited data from a phase 2 trial of the anti-CD3 agent teplizumab for type 1 diabetes prevention in those with ≥ 2 islet autoantibodies and abnormal glucose tolerance. According to the ADA, “The question for this study is whether treatment at early stages of disease can delay progression to clinical (stage 3) type 1 diabetes.” Two-year clinical results from TrialNet’s low-dose ATG-GSCF trial in new-onset diabetes will also be presented as well as mechanistic data from TrialNet’s natural history and immune effects of oral insulin studies. These important results and mechanistic studies will be presented on Sunday June 9 from 8:00 to 10:00 am.
And for the first time, ADA has listed all of these trials on its 79th Scientific Sessions homepage under “highly anticipated study announcements of 2019.”

The Latest From CVOTs: REWIND, CAROLINA, and DECLARE-TIMI 58

As usual, the latest crop of CVOT results will each have their own 2-hour sessions. On Sunday June 9 at 2:15 pm, new data will be presented from the Dapagliflozin Effect on Cardiovascular Events (DECLARE-TIMI 58) study, the first CVOT to enroll a much broader and healthier population of patients with type 2 diabetes — those without pre-existing cardiovascular disease but with multiple risk factors — as well as some patients with pre-existing cardiovascular disease.
Primary results from the trial were presented in November at the American Heart Association (AHA) Scientific Sessions 2018 and showed that dapagliflozin significantly reduced hospitalizations for heart failure and nonsignificantly reduced major adverse cardiovascular events (MACE).
At ADA, those results will be reviewed along with new subanalyses, renal endpoints, and safety data for the SGLT2 inhibitor.
Next, on Sunday June 9 at 4:30 pm, comes the Researching CV Events With a Weekly Incretin in Diabetes (REWIND) trial, with 5-year results for dulaglutide, a once-weekly injectable GLP-1 agonist, in a large population of lower-risk adults. This is the first such study with a GLP-1 agonist to include a majority of patients who did not have established cardiovascular disease at baseline.
Top-line results from REWIND, announced in November 2018, showed dulaglutide significantly reduced the risk of MACE.
And on Monday June 10 at 4:30 pm, data will be presented from the Cardiovascular Safety of Linagliptin (CAROLINA) study, the longest CVOT so far (8 years) and the only one to include a head-to-head active comparator (the sulfonylurea glimepiride). In addition to the findings for linagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor, the results may also inform the longstanding debate about the cardiovascular safety of sulfonylureas.

Oral Semaglutide: A Game Changer?

A session on Tuesday morning at 9:45 am will cover the PIONEER program trials for oral semaglutide, the GLP-1 receptor agonist already approved as a once-weekly injectable.
Top-line results for PIONEER 6, announced in November 2018, showed reductions in cardiovascular and all-cause mortality but not the overall composite primary MACE endpoint.
Previously reported results from the PIONEER series of trials include PIONEER-1, which demonstrated the oral version’s glucose-lowering and weight loss capabilities, while in PIONEER-3 the drug reduced HbA1c more than sitagliptin.
Philipson commented, “Semaglutide has been on the market for some time but we’ve never had an oral [GLP-1 agonist]…before…I think this is a very big deal and potentially game changing for people with type 2 diabetes, so I’m very excited about that.”
“How much the oral semaglutide can recapitulate the benefits of the injected one is critical,” he stressed.

Proving Prevention: Vitamin D, Medications, and Lifestyle Interventions    

On Saturday June 8 at 4:00 pm, results from the Prevention of Diabetes in Europe and Around the World (PREVIEW) study, the largest-ever (N = 2326) to investigate diabetes prevention through lifestyle interventions, will be reviewed.
Data from PREVIEW, previously reported at the European Association for the Study of Diabetes (EASD) 2018 Annual Meeting, suggested a 2-month weight loss regimen using meal substitutes followed by long-term weight maintenance through diet and exercise may be an optimal approach to preventing type 2 diabetes through lifestyle.
Another prevention study, the multicenter Vitamin D and Type 2 Diabetes (D2d) clinical trial, supported by the National Institutes of Health, is the largest ever study specifically designed to determine whether vitamin D supplementation can reduce the risk of developing type 2 diabetes among people at risk. Final results will be presented on Friday at 11:30 am.
“There’s been a lot of epidemiological evidence that vitamin D is helpful for either beta-cell function or insulin action, but there’s never been a real randomized prospective trial, particularly for type 2 diabetes prevention,” Florez explained.
And Philipson commented, “This is a hot topic in diabetes…Many of us are measuring vitamin D levels and supplementing, but should we be? It’s not always reimbursed. Right now clinicians are deciding on their own.”
On Sunday at noon, results will be presented from the Adult Medication studyof the three-part Restoring Insulin Secretion (RISE) program looking at both prevention and early treatment of type 2 diabetes.
The RISE pediatric medication study, presented at ADA last year, showed that in adolescents with impaired glucose tolerance (prediabetes) or recent-onset type 2 diabetes, early intervention with long-acting insulin followed by metformin or metformin alone — both given for a year — failed to prevent deterioration of beta-cell function.
“These are really critical studies for our understanding of what’s happening in type 2 diabetes,” Philipson emphasized.

Kidney and Cardio: Latest Data from CREDENCE and CARMELINA

A single 2-hour session on Tuesday starting at 7:30 am will review data from the landmark Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation (CREDENCE) trial, which assessed progression of kidney disease and secondarily cardiovascular outcomes, and the Cardiovascular and Renal Microvascular Outcome Study with Linagliptin (CARMELINA), which assessed cardiovascular outcomes and secondarily kidney disease progression.
Primary findings from CREDENCE, presented in April at the International Society of Nephrology (ISN): 2019 World Congress, showed canagliflozin lowers the risk for progression to end-stage renal disease by 30% in patients with type 2 diabetes and chronic kidney disease, as well as lowers the risk for MACE.
And data from CARMELINA, first presented in October 2018 at the EASD meeting, showed adding linagliptin to standard of care in patients with type 2 diabetes at high cardiovascular risk did not worsen cardiovascular, heart failure, or renal events, even in those who already had kidney disease.
Key findings from both trials will be reviewed and new analyses presented.
“CREDENCE and CARMELINA are very big deals,” Philipson underlined. “These are follow-up studies that will help affirm the original report. They’re really exciting.”

A Tough Subject: Type 2 Diabetes in Youth

On Saturday June 8 at 1:45 pm, a 2-hour session will be devoted to the latest findings from the follow-up to the multicenter, multi-ethnic, randomized Treatment Options for type 2 Diabetes in Adolescents and Youth (TODAY) study.
The post-intervention follow-up, TODAY2, is tracking the youth into young adulthood to investigate rates of renal, cardiac, eye, and nerve complications, as well as pregnancy outcomes and healthcare utilization.
Philipson commented, “If there’s one ray of light that comes from this study it would be wonderful. But we have a strong feeling that children with type 2 diabetes actually do worse in some cases than children with type 1. It can be a profound disease that leads to early death, and in many cases we don’t even have a good approach to treating it. These talks will give us some indication of the outcomes of the study and what we might learn.”

Venture Outside Your Comfort Zone

Of course there’s much, much more to the meeting. Other highlights include sessions on the rational use of opioids for treating painful diabetic neuropathy, learning from atypical diabetes, an ADA consensus paper on nutrition therapy for adults with diabetes, new artificial pancreas trial results, and two keynote award lectures on obesity that “will be more clinical than usual,” Philipson observed.
Both Philipson and Florez urge delegates to attend sessions that may be outside their usual areas of focus.
Referring to the nutrition session, held under the “Behavioral Medicine, Clinical Nutrition, Education, and Exercise” track, Florez said, “We tend to just go to sessions that are in our comfort zones. But if you’re a clinician who takes care of people with diabetes you can’t just leave it to the nutritionists and the [certified diabetes educators] to attend this track on behavioral medicine and clinical nutrition.”
“I think it’s incumbent on all of us who take care of diabetes…to be up to date on the latest in nutrition therapy…This disease requires a multidisciplinary, multipronged approach. Physicians need to go beyond drugs to other forms of therapy. Don’t use the meeting to go over things you already know.”
Indeed, said Philipson, “I encourage people to go to lectures and meetings they wouldn’t normally go to…This meeting is really for everybody with an interest in diabetes, from basic scientists to practitioners, whether they’re MDs or psychologists or exercise physiologists, ophthalmologists, etc. That breadth is unmatched by any other meeting that includes diabetes.”
Florez has consulted for Janssen. Philipson has received research funding from Janssen, ADA, JDRF, Helmsley Foundation, and National Institutes of Health.

Insulin-Producing Beta Cells Are Not Irreversibly Lost in Early Type 2 Diabetes

Analysis of data over a two-year period finds losing weight and minimizing weight regain can potentially lead to remission of type 2 diabetes
Pancreatic beta cells that do not produce sufficient insulin in people with type 2 diabetes (T2D) are not permanently damaged during the early stages of the disease and can be restored to normal function through the removal of excess fat in the cells, according to a study entitled “Remission of Type 2 Diabetes for Two Years Is Associated with Full Recovery of Beta-Cell Functional Mass in the Diabetes Remission Clinical Trial (DiRECT)” presented today at the American Diabetes Association’s® (ADA’s) 79th Scientific Sessions®. More than one-third (36%) of the participants who took part in an intensive weight management program saw remission of their T2D after two years.
Type 2 diabetes is a progressive disease over time, and previous research has suggested beta cell death is the root cause of increasing failure of insulin-production and severity of T2D. Findings presented today examined beta cell production within a geographically-defined subgroup of the original DiRECT participants who had already achieved remission of T2D through diet-induced weight loss. The study found, however, beta cells are not permanently damaged in early T2D and can be rescued by removing the metabolic stress of excess fat within the cells. The findings are the result of the examination of insulin production on a subgroup at baseline (starting weight), immediately after weight loss (five months), and upon follow up of one and two years. Researchers defined participants as “in remission” if long-term blood glucose levels (HbA1c) were less than 48mmol/mol (6.5%) and their fasting glucose plasma (FPG) levels were less than 126mg/dl, without the use of any T2D medications.
The researchers used a Stepped Insulin Secretion Test with Arginine (SISTA) to quantify functional beta cell mass (maximum insulin secretory response during hyperglycemia). Insulin secretion rates were estimated by de-convolution, and participants’ A1C and fasting plasma glucose (FPG) levels were assessed. Analysis determined that many from the group who had initially achieved remission of T2D – blood glucose levels capable of achieving non-diabetic blood glucose control although not considered normal – had remained in remission two years after the study. Within the 40 people who had initially achieved remission of T2D, 20 participants (13 male/seven female) remained in remission, 13 gained weight and relapsed, and seven did not maintain follow-up. Furthermore, when compared to a nondiabetic comparator (NDC) group used in the study, which matched the age/gender of the DiRECT intervention group participants after weight loss, the study participants’ maximum rate of insulin secretion was comparable. The intervention group participants’ insulin secretion increased from a median of 0.58 nmol/min/m2 at baseline to 0.94 nmol/min/m2 after two years, and the insulin secretion of the NDC group had a median insulin secretion rate of 1.02 nmol/min/m2 at 24-months follow up.
DiRECT is the latest in a series of studies to test the 2008 Twin Cycle hypothesis. Research released in 2011 reported a dramatic fall in liver fat and a significant decrease in intra-pancreatic fat levels following 33 pounds of weight loss with recovery of some beta cell function in people with T2D. In 2016, scientists reported that maintaining a healthy weight for nine months after a period of weight loss assisted in beta cell recovery. The open-labeled, cluster-randomized controlled trial involved 306 participants from 49 primary care practices in Scotland and England between 2014 and 2017. Patients ranged in ages from 20 to 65, had a body mass between 27-45 kg/m 2, were not receiving insulin and with up to six years duration of T2D. Practices were randomly selected to offer participants one of two treatments, both of which had already been shown to be effective. DiRECT aimed to ascertain which treatment option was more effective.

More Anti-Obesity Drugs for Teens Coming, Devices Are Next Step

Few medical therapies have been approved to treat adolescents with obesity but that is about to change, and a next step will be to test endoscopic devices in teens, two experts have predicted here at the American Diabetes Association (ADA) 2019 Scientific Sessions.
“I think there is a place for medication in adolescent obesity,” but current options “continue to remain limited,” Daniel S. Hsia, MD, Pennington Biomedical Research Center, Baton Rouge, Louisiana, summarized to Medscape Medical News following his presentation here.
He had explained that only orlistat and phentermine are approved by the US Food and Drug Administration (FDA) to treat adolescents with obesity, whereas nine medical therapies have been approved for weight loss in adults.
“I think that off-label use is going to continue until we have more pediatric adolescent data and we have FDA approvals for [anti-obesity] medications” for adolescents, Hsia predicted.
However, “there is hope on the horizon,” he added, “for the specific [obese young] populations that need medical therapy that may not fit so much in bariatric surgery or may not have had quite the benefit from lifestyle modification.”
Liraglutide (Saxenda, Novo Nordisk) [trial] results [in teens] will probably be available early next year,” Hsia expects. “That’s probably the one that will be the next one up,” to be approved for treating adolescents with obesity, he said.
A randomized controlled trial of lorcaserin (Belviq, Eisai) in adolescents with obesity is ongoing and still open for enrolment, he noted, and there is a phase 4 trial that is just starting for phentermine/topiramate (Qsymia, Vivus).
During the same session, Andrew C. Storm, MD, Mayo Clinic, Rochester, Minnesota, summarized the growing number of endoscopic devices that are approved or being tested for weight loss.
The approvals have happened “in the past 3 to 4 years and three to five have FDA approval trials ongoing or starting within the summer [in adults], so I expect to see — if not this year then definitely in the next year or two — quite a number of endoscopic therapies for obesity and metabolic disease available,” he told Medscape Medical News.
“It is pretty clear that obesity from childhood carries into adulthood,” Storm added. “Given that these [devices] are so safe and have such reasonable impacts in obesity upfront, I think the next step will be studying them in young adults.”
“It’s very exciting because there are new and evolving therapies in the field of the treatment of obesity [for adolescents],” session chair Amy E. Rothberg, MD, PhD, University of Michigan, Ann Arbor, told Medscape Medical News.
“It’s going to reshape the landscape and practitioners will be more comfortable prescribing these therapies,” she predicted.
“Stay tuned, but there are probably going to be double what we have in terms of pharmacotherapy and combination pharmacotherapy in the future” for treating adolescents, she said.
Asked if this will this make a dent in the obesity rate in young people, she replied: “I’m optimistic, so I certainly hope so.”

Only Orlistat and Phentermine Approved for Obese Teens

Endocrine Society guidelines published in 2017 (J Clin Endocrinol Metab2017;102:709-757) specify that pharmacotherapy with FDA-approved therapies can be suggested for adolescents who are obese if a formal lifestyle modification program fails to limit weight gain or improve comorbidities, Hsia noted.
The guidelines also advise discontinuing therapy if the patient does not achieve a greater than 4% reduction in body mass index (BMI)/BMI z-score by 12 weeks.
Orlistat is the only FDA-approved medication for long-term use in adolescents age 12 years or older, and it is associated with a 0.7 to 1.7 kg/mreduction in BMI. However, because of side effects of fecal urgency/incontinence and fatty/oily stools, it is of limited clinical use in this age group.
Phentermine, which suppresses appetite, is approved by the FDA for 12 weeks or less in individuals age 16 years and older. However, it may cause increased blood pressure and heart rate, and there are limited safety and efficacy data in adolescents.
Anti-obesity pharmacotherapies for adults included four drugs approved in the 1950s for short-term use, and the one most commonly still in use is phentermineHsia explained.
More recently, in 1999 to 2014, the FDA approved five drugs for long-term use for weight loss: Orlistat (Xenical), lorcaserin (Belviq), phentermine/topiramate(Qsymia)bupropion/naltrexone (Contrave), and liraglutide, a subcutaneous injectable glucagon-like peptide 1 (GLP-1) agonist first approved for type 2 diabetes (as Victoza, Novo Nordisk) but subsequently approved for obesity as Saxenda.
And when used off-label in adolescents, the type 2 diabetes agent metformindecreases BMI by about 1.2 kg/m2 over 6 to 12 months and the GLP-1 agonist exenatide decreases BMI by 1.1 to 1.7 kg/m2 over 3 months.
Similarly, off-label use in adolescents of antiepileptic drugs (topiramate and zonisamide) decreases BMI by about 1.3 to 4.1 kg/m2 over 6 months; growth hormone decreases fat mass in Prader-Willi syndrome; and octreotide may provide weight stabilization in hypothalamic obesity.
Moreover, three drugs approved in adults are currently being investigated in trials in adolescents: lorcaserin (Belviq) 20 mg/day is being studied in a 52-week randomized controlled trial in 12 to 17 year olds; phentermine/topiramate (Qsymia) is being studied in a 56-week phase 4 randomized controlled trial in 12 to 16 year olds; and liraglutide (Saxenda) is being studied in a 56-week trial in 12 to 17 year olds.
And in future, combination pharmacotherapy may come to the fore, as it may allow lower dosing of two drugs with different mechanisms, which might mitigate side effects, Hsia said.
Newer agents in the pipeline include centrally acting agents, gut hormone and incretin targets, leptin analogs, and dual-action GLP-1/glucagon receptor analogs.

Growing Number of Endoscopy Devices

Meanwhile, Storm explained that the number of “devices, techniques, and providers are growing to meet the demand of the obesity pandemic,” and there is strong level 1 evidence that endoscopic bariatric therapies can help patients achieve significant weight loss and metabolic improvement.
These devices are safe and cost-effective, and the procedures can be repeated.
FDA-approved intragastric balloons include OrberaReshape (a dual balloon system), and Obalon (a gas-filled balloon that is swallowed), which delay gastric emptying and have to be removed after 6 months.
And a pivotal trial is being conducted to obtain FDA approval for an investigational gastric balloon that could stay in place for 12 months, Storm noted.
The FDA has already approved endoscopic sleeve gastroplasty, a type of gastric remodeling that is “probably the most exciting” and “most promising” endoscopic technique, according to Storm, that reshapes the stomach down to the size of a banana, which is similar to bariatric sleeve gastrectomy but uses a minimally invasive procedure.
Another type of gastric remodeling, the primary obesity surgery endolumenal (POSE) procedure, is not yet approved.
Aspiration therapy, on the other hand, has received FDA approval.
And the FDA recently approved Gelesis100 (Plenity, Gelesis) hydrogel capsules, Rothberg added, as previously reported. “We’ll see in post-marketing data how that fares,” she noted.
“The big question,” Storm said, “is how to combine [endoscopic devices] with medication to achieve bariatric surgery levels of weight loss.”
ADA 2019 Scientific Sessions. Presented June 7, 2019.
Hsia has reported serving as principal investigator for studies sponsored by Novo Nordisk and Vivus, with funds paid directly to his institution. Storm has reported consulting for GI Dynamics and receiving research support from Boston Scientific.