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WB-001

Alternative Names: WB-001, WB001
Latest Update: 2023-07-19
Latest Update Note: Clinical Trial Update

Product Description

The WB001 treatment consists of PPD-specific psychoeducational lessons and CBT-specific skills or tools. The lessons teach PPD-specific information to normalize and contextualize postpartum experiences, as well as provide information on effective mood management and mental health promotion in the context of having recently given birth. Patients complete up to 30 psychoeducational lessons. In addition, patients access and apply core CBT-based tools upon endorsing a negative mood. These tools are core to CBT and are considered transdiagnostic. Examples include thought challenging, behavioral activation, mindfulness, and self-care. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT04576754?term=wb001&draw=2&rank=1)

Mechanisms of Action: Device

Novel Mechanism: No

Modality: Device

Route of Administration: N/A

FDA Designation: Breakthrough Therapy - Depression, Postpartum *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Woebot Health
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for WB-001

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

WB001-001

N/A

Terminated

Depression, Postpartum

2023-05-10

Pivotal Test

N/A

Completed

Depression, Postpartum

2021-06-14

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