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Efficacy, tolerability, and cognitive effects of deep transcranial magnetic stimulation for late-life depression: a prospective randomized controlled trial

Key Takeaway: A study on high-dose deep rTMS for late-life depression found significant efficacy, with a remission rate of 40% compared to 14.8% in the sham group. The treatment was safe and well tolerated, with no serious adverse events. However, pain was reported more frequently in the active treatment group, highlighting a potential drawback.
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POSITIVE FACTORS

  • High-dose deep rTMS shows significant efficacy in treating late-life depression.
  • Remission rates were notably higher in the active treatment group.
  • The treatment was found to be safe and well tolerated.
  • No serious adverse events were reported.

CONCERNS & RISKS

  • Pain was reported more frequently in the active treatment group.
  • Limited treatment options for late-life depression remain a concern.

Full Press Release Details

Background:
Late-life depression (LLD) is a growing worldwide problem due to demographic changes, with limited treatment options due to high rates of pharmacotherapy adverse effects, accessibility of psychotherapy, and tolerability of electroconvulsive therapy. Novel neuromodulation techniques, such as repetitive transcranial magnetic stimulation ( rTMS ), may overcome these limitations.
Objective:
The objective of this study is to determine the efficacy, tolerability, and cognitive effects of high-dose deep rTMS in LLD.
Methods:
In this study we randomized older adults between 60 and 85 years old with major depressive disorder (MDD) to sham or active deep rTMS (H1 coil, 6012 pulses, 18 Hz, 120% of resting motor threshold) delivered over the dorsolateral and ventrolateral prefrontal cortex 5 days per week over 4 weeks. Our primary outcome was remission of depression in an intention-to-treat analysis. We also assessed change in cognitive functioning with rTMS treatment and tolerability based on adverse effects.
Results:
Fifty-two participants were randomized to active (n =25) or sham H1 coil (n=27). Remission rate was significantly higher with active than sham rTMS (40.0% vs 14.8%) with a number needed to treat of 4.0 (95% CI: 2.1–56.5). There was no change on any measure of executive function and no serious adverse events. Adverse effect profiles were similar between active and sham rTMS , except for reports of pain being significantly more common in the active condition (16.0% vs 0%).
Conclusions:
High-dose deep rTMS appears to be safe, well tolerated, and efficacious in the treatment of LLD.

Frequently Asked Questions

What was the objective of the deep rTMS study?

The study aimed to determine the efficacy, tolerability, and cognitive effects of high-dose deep rTMS in late-life depression.

What were the remission rates for active vs sham rTMS?

The remission rate was 40% for active rTMS compared to 14.8% for sham treatment.

How was the treatment administered in the study?

Participants received deep rTMS 5 days a week for 4 weeks, targeting specific brain areas.

Were there any serious adverse events reported?

No serious adverse events were reported during the study.

What was a common adverse effect noted in the study?

Pain was reported significantly more often in the active rTMS group.

Last updated: Jun 17, 2024