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FDA Panel Rejects Combo Drug for PTSD
FDA Panel Rejects Combo Drug for PTSD

Medscape

time7 days ago

  • Health
  • Medscape

FDA Panel Rejects Combo Drug for PTSD

An FDA advisory panel has resoundingly rejected the supplemental new drug application for the atypical antipsychotic brexpiprazole (Rexulti, Otsuka Pharmaceutical Co., Ltd.), in combination with the selective serotonin reuptake inhibitor (SSRI) sertraline, for the treatment of adults with posttraumatic stress disorder (PTSD). Based on the data at hand, in a 10 to 1 vote, the Psychopharmacologic Drugs Advisory Committee felt that the efficacy of brexpiprazole, when started concurrently with sertraline, has not been established in PTSD. In a briefing document released ahead of the FDA committee meeting, FDA reviewers flagged 'discordant' results from the two phase 3 trials. They noted that while study '071' was 'robustly positive,' study '072' was 'clearly and convincingly' negative and failed to demonstrate statistical significance on its primary or secondary endpoints. Given the conflicting phase 3 results, the company also provided the FDA with data from the '061' phase 2 study. However, the reviewers cited statistical and methodologic concerns with this study. The data from this study were 'retrospectively analyzed with post hoc multiplicity control methods to provide additional efficacy evidence, raising concerns about type I error inflation,' the reviewers cautioned. The committee also had concerns about the 061 data analysis. Taken together, the data 'is not crossing that bar in my head,' said committee member Jess Fiedorowicz, MD, PhD, head of the Department of Mental Health, The Ottawa Hospital, Ottawa, Ontario, Canada. Walter Dunn, MD, PhD, director, Mood Disorders Section, West Los Angeles Veterans Affairs Medical Center, Los Angeles, agreed. Dunn said while he is a 'strong advocate' for increasing treatment options for PTSD, he was 'not convinced' of the efficacy of the combination given the conflicting data. Murray Raskind, MD, professor, Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, felt it would be 'hard to translate the confusing contradictory datasets to my clinical practice.' Raskind also said he is not convinced the combination offers clinicians a new tool. Brexpiprazole is currently approved as adjunctive treatment of major depressive disorder in adults, treatment of schizophrenia in adults and adolescents aged 13 years or older, and treatment of agitation associated with Alzheimer's dementia. 'We already have sertraline, and we already have brexpiprazole. The prescribing physician can make the decision to progress to the combination or start with it in the patient with PTSD,' Raskind said. Other committee members agreed. Committee members in general felt that in the real world, co-initiation of both drugs may not be the preferred approach. It's more likely that clinicians would opt to start sertraline first, then add brexpiprazole if needed. 'Third-party payers may require that,' Dunn predicted. During the public comment period, Michael Abrams, PhD, MPH, senior health researcher with Public Citizen, said the data supporting the use of this combination for treatment of PTSD is 'weak at best, based on two conflicting phase 3 trials and a questionable post hoc analysis of data from a phase 2 trial,' and he urged the committee and the FDA to reject the combination. The lone 'yes' vote for the brexpiprazole-sertraline combination in PTSD came from the patient advocate on the committee, Laura Block, PharmD, clinical pharmacist (retired), Cary, North Carolina. Block noted that while both of these individual component drugs are on the market, a third-party payer isn't likely to pay without an FDA-approved indication. 'That means that there are those who are going to have difficulty accessing,' Block commented. At the same time, Block said she would not want to offer patients 'destructive false hope,' and whether it is approved, she would like to see either a phase 3 or phase 4 study. Currently, the SSRI sertraline and paroxetine are the only FDA-approved medications for PTSD, and while these medications can be effective, many patients fail to achieve remission or discontinue treatment due to side effects or lack of response. The proposed upfront co-initiation of brexpiprazole with sertraline is a novel treatment paradigm. If approved by the FDA, it would be the first new treatment for PTSD in more than 20 years. The FDA is not required to follow the advice of its advisory committees, but it often does.

Japan economic panel urges $400 billion investment to boost SME productivity
Japan economic panel urges $400 billion investment to boost SME productivity

CNA

time14-05-2025

  • Business
  • CNA

Japan economic panel urges $400 billion investment to boost SME productivity

TOKYO :Japanese Prime Minister Shigeru Ishiba's economic advisory panel recommended investment of $400 billion to boost productivity at smaller firms, a crucial segment in the government's quest to achieve wage growth well in excess of inflation. The panel, tasked to compile key economic policies for the government, presented a five-year plan at its meeting on Wednesday outlining steps to help small and mid-sized enterprises (SMEs) raise wages. SMEs, which employ 70 per cent of Japan's workforce, have been struggling to consistently increase pay as they are already spending more of their profits on wages than their bigger counterparts. Pay hikes are seen as pivotal to retaining and attracting talent, particularly for SMEs, in the face of severe labour shortages. The five-year plan sets the goal of stably achieving real wage increases of 1 per cent higher than inflation, a bullish target given Japan's inflation-adjusted real wages have struggled to sustainably turn positive for decades. The specific steps include public and private-sector investment of 60 trillion yen ($407.86 billion) over the next five years to allow SMEs to digitise or automate operations, as well as beefing up support to foster mergers and acquisitions. The panel also suggested strengthening regulatory scrutiny over business practices typically targeted at larger firms' tendency to pressure their suppliers not to raise prices. The panel's proposals will be included in the annual policy guidelines to be released around June. The panel was launched by former Prime Minister Fumio Kishida in 2021 to formulate a strategy to tackle wealth disparities and redistribute wealth to households in a "new capitalism" programme. Ishiba has upheld his predecessor's new capitalism policy drive, focusing on getting the economy to fully shake off the deflation mindset that has hobbled it since the 1990s. ($1 = 147.1100 yen)

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