Long-term Asenapine Well-tolerated And Effective Treatment Option for Schizophrenia

Written By :  Dr. Kamal Kant Kohli
Published On 2023-08-22 03:45 GMT   |   Update On 2023-08-22 08:13 GMT

Schizophrenia is a severe and disabling mental disorder affecting 0.5% to 1.5% of adults, characterized by a range of symptoms including positive, negative, and cognitive impairments. The debilitating nature of this disorder often leads to reduced social functioning and overall quality of life for patients. In the quest for effective treatments, a recent study published...

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Schizophrenia is a severe and disabling mental disorder affecting 0.5% to 1.5% of adults, characterized by a range of symptoms including positive, negative, and cognitive impairments. The debilitating nature of this disorder often leads to reduced social functioning and overall quality of life for patients. In the quest for effective treatments, a recent study published in Neuropsychopharmacology Reportsby Toshihiko Kinoshita and colleagues has examined the potential benefits of long-term treatment with asenapine, a second-generation antipsychotic.

Second-generation antipsychotics are known for their ability to target multiple receptors, including dopamine and serotonin receptors, resulting in improved management of a broader spectrum of symptoms compared to first-generation antipsychotics. While these drugs are generally associated with fewer extrapyramidal side effects, they do come with their own set of challenges, such as weight gain and hyperprolactinemia.

The study, which followed an initial 6-week double-blind trial of asenapine sublingual tablets in Asian patients with acute exacerbation of schizophrenia, assessed the safety and efficacy of a 52-week treatment period using flexible doses of asenapine. The subjects consisted of 201 individuals, including 44 who initially received a placebo (P/A group) and 157 who received asenapine (A/A group) in the previous trial.

The results revealed the following key findings:

● Adverse events were reported in 90.9% of the placebo group and 85.4% of the asenapine group, showcasing that long-term asenapine treatment is well-tolerated.

●  Serious adverse events occurred in 11.4% of the placebo group and 20.4% of the asenapine group.

● No significant changes were observed in body weight, body mass index, or measurements related to glycated haemoglobin, fasting plasma glucose, insulin, and prolactin levels.

● The Positive and Negative Syndrome Scale (PANSS) total score and other measures indicated a sustained efficacy rate of around 50% between 6 and 12 months of asenapine treatment.

The study's outcomes suggest that long-term treatment with asenapine not only maintains its efficacy but also offers a well-tolerated option for patients with schizophrenia. The ability to sustain the positive effects of the drug while minimizing adverse effects is encouraging, as it signifies a potential path toward improving the quality of life for individuals grappling with this challenging disorder.

Asenapine's ability to address a broader range of symptoms beyond positive ones, including negative symptoms and cognitive impairment, underscores its potential to positively impact patient social reintegration and overall quality of life. While challenges remain, the findings are a promising step toward enhancing the long-term management of schizophrenia.

It is essential to further validate these results through larger and longer-term studies to establish the safety and efficacy of asenapine in a wider population and under different conditions. These findings highlight the continuous efforts in the field of psychiatry to refine treatment strategies and offer better solutions for patients with schizophrenia.

Reference:

Kinoshita, T., Takekita, Y., Hiraoka, S., Tamura, F., & Iwama, Y. (2023). Long‐term safety and efficacy of sublingual asenapine for the treatment of schizophrenia: A phase III extension study with follow‐up for 52 weeks (P06125)—Secondary publication. Neuropsychopharmacology Reports. https://doi.org/10.1002/npr2.12342

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Article Source : Neuropsychopharmacology Reports

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