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Report Overview

Postpartum depression (PPD) is a serious mood disorder that affects women after childbirth. According to Samar A. Amer et al. (2024), it impacts around 10 % of women, or about 1 in 7. Traditional therapies include SSRIs, hormonal treatments, cognitive-behavioral therapy, and interpersonal therapy. According to the postpartum depression drug pipeline analysis by Expert Market Research, there is a growing focus on developing rapid-acting neuroactive steroids (such as zuranolone) and novel molecules. Pipeline growth is expected to accelerate in the coming years, driven by increasing awareness, regulatory support, and unmet clinical need.

  • Major companies involved in the postpartum depression pipeline analysis include Lipocine Inc., Nanjing Minova Pharmaceutical Co., Ltd., and others.

  • Leading drugs currently in the pipeline include LPCN 1154A, HS-10353, KH607, and others.

  • Rising clinical trial activity, growing focus on novel neurosteroid-based therapies, and increased regulatory approvals are expected to accelerate the development and commercialization of innovative treatments in the coming years.

Report Coverage

The Postpartum Depression Pipeline Analysis Report by Expert Market Research gives comprehensive insights into postpartum depression therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for postpartum depression. The postpartum depression report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The postpartum depression pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with postpartum depression treatment guidelines to ensure optimal care practices.

The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to postpartum depression.

Postpartum Depression Pipeline Analysis By Drug Class

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Postpartum Depression Pipeline Outlook

Postpartum depression (PPD) is a severe mood disorder that typically develops after childbirth but can also arise during late pregnancy. It is characterized by persistent sadness, anxiety, guilt, fatigue, and loss of interest in daily activities, often caused by hormonal changes, emotional stress, and physical exhaustion. PPD can disrupt the maternal-infant bond and affect both the mother's and child’s overall well-being.

Treatment for postpartum depression includes antidepressant medications, hormonal therapy, and psychotherapy to restore emotional balance and improve quality of life. In August 2023, the U.S. Food and Drug Administration approved Zurzuvae (zuranolone), the first oral medication for PPD, developed by Sage Therapeutics, Inc., representing a major milestone in the postpartum depression treatment landscape and expanding therapeutic accessibility for affected women.

Postpartum Depression Epidemiology

According to Samar A. Amer et al., 2024, postpartum depression (PPD) affects around 10% of women after childbirth, with nearly 50% of cases remaining undiagnosed. As per global estimates, the prevalence is about 17.22%, reaching up to 15% in eighty different countries. According to Sajna Panolan et al., 2024, the overall prevalence of PPD in India is 22%, with the highest rate of 26% in southern regions and the lowest rate of 15% in northern regions. As per Nehaa Khadka et al., 2024, global prevalence ranges between 10% and 20%, and about 13% in the United States. These statistics highlight the pressing need for improved screening and therapeutic interventions in postpartum care.

Postpartum Depression – Pipeline Therapeutic Assessment

This section of the report covers the analysis of postpartum depression drug candidates based on several segmentations, including:

By Phase

The pipeline assessment report covers 50+ drug analyses based on phase:

  • Late-Stage Products (Phase 3 and Phase 4)
  • Mid-Stage Products (Phase 2)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

By Drug Class

The postpartum depression pipeline analysis report covers 50+ drug analyses based on drug classes:

  • Small Molecules
  • Monoclonal Antibodies
  • Gene Therapies
  • Peptides
  • Polymers

By Route of Administration

The pipeline assessment report covers 50+ drug analyses based on the route of administration.

  • Oral
  • Parenteral
  • Others

Postpartum Depression Pipeline Assessment Segmentation, By Phases

The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total postpartum depression clinical trials, holds 43%, reflecting robust research and promising therapeutic advancements. Phase III accounts for 22%, while phase IV contributes 17%, indicating strong ongoing clinical validation. Phase I represents 13% highlighting continuous innovation in the therapeutic landscape.

Postpartum Depression Pipeline Assessment Segmentation, By Drug Classes

The drug molecule categories covered under the postpartum depression pipeline analysis include small molecules, monoclonal antibodies, gene therapies, peptides, and polymers. The postpartum depression report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for postpartum depression. Antidepressant drug classes in the postpartum depression pipeline are advancing to address unmet therapeutic needs. For instance, Minoview Pharmaceuticals’ MI078 capsule, a novel oral antidepressant, has completed Phase II clinical trials. The drug demonstrated significantly higher efficacy than placebo, achieving primary endpoints within three days of administration, indicating strong potential as a fast-acting treatment option for postpartum depression.

Postpartum Depression Clinical Trials – Key Players

The EMR report for the postpartum depression pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a detailed postpartum depression therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in postpartum depression clinical trials:

  • Lipocine Inc.
  • Nanjing Minova Pharmaceutical Co., Ltd.
  • Hansoh Pharmaceutical Co., Ltd.
  • DuKang Pharmaceuticals, Inc.
  • Chengdu Kanghong Pharmaceutical Group Co., Ltd.
  • Biogen
  • Supernus Pharmaceuticals, Inc.
  • Reunion Neuroscience Inc.
  • Bristol-Myers Squibb
  • Brii Biosciences Limited

Postpartum Depression – Emerging Drugs Profile

This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for postpartum depression. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of postpartum depression drug candidates.

Drug: LPCN 1154A

LPCN 1154A is an oral formulation of brexanolone being developed by Lipocine Inc. for the treatment of severe postpartum depression. This Phase 3 randomized, blinded, placebo-controlled study is evaluating the safety and efficacy of LPCN 1154A in reducing depressive and anxiety symptoms among women with severe PPD. The study is also examining the tolerability and side effects of the drug. LPCN 1154A is designed to offer a convenient, at-home alternative to current hospital-based therapies, promoting faster recovery and uninterrupted maternal bonding.

Drug: HS-10353

HS-10353 is an investigational GABA receptor positive allosteric modulator being developed by Jiangsu Hansoh Pharmaceutical Co., Ltd. for treating postpartum depression (PPD). This Phase II randomized, double-blind, placebo-controlled study is evaluating the drug’s ability to reduce depressive symptoms and improve emotional stability. HS-10353 works by enhancing GABAergic signaling, correcting receptor dysfunction, and restoring balance between GABA and NMDA receptors, which are crucial for mood regulation. Administered orally at night for 14 days, it is expected to deliver rapid, sustained antidepressant effects with a favorable safety and tolerability profile.

Drug: KH607

KH607 is a novel positive allosteric GABAA receptor modulator being developed by Chengdu Kanghong Pharmaceutical Group Co., Ltd. for the treatment of postpartum depressive disorder. This Phase 2 clinical trial is evaluating the efficacy, safety, and pharmacokinetics of KH607 in 72 women diagnosed with postpartum depression. The study is using a randomized, double-blind, placebo-controlled design. KH607 demonstrates high oral bioavailability and potent activity, effectively penetrating the blood-brain barrier to deliver strong anti-anxiety and antidepressant effects.

*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*

Key Questions Answered in the Postpartum Depression Pipeline Insight Report

  • Which companies/institutions are leading the postpartum depression drug development?
  • Which company is leading the postpartum depression pipeline development activities?
  • What is the current postpartum depression commercial assessment?
  • What are the opportunities and challenges present in the postpartum depression pipeline landscape?
  • What is the efficacy and safety profile of postpartum depression pipeline drugs?
  • Which company is conducting major trials for postpartum depression drugs?
  • Which companies/institutions are involved in postpartum depression collaborations aimed at providing enhanced therapeutic alternatives for patients?
  • What are the geographies covered for clinical trials in postpartum depression?

Reasons To Buy This Report

The Postpartum Depression Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for postpartum depression. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into postpartum depression collaborations, regulatory environments, and potential growth opportunities.

Related Reports

Global Clinical Trials Market

Postpartum Depression Epidemiology Forecast

*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*

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Report Summary

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Key Highlights of the Report

Please note that the figures mentioned in the description serve as estimates and may vary from the actual figures presented in the final report.

Scope of the Report

Details

Drug Pipeline by Clinical Trial Phase

  • Late-Stage Products (Phase III and Phase IV)
  • Mid-Stage Products (Phase II)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

Route of Administration

  • Oral
  • Parenteral
  • Others

Drug Classes

  • Small Molecules
  • Monoclonal Antibodies
  • Gene Therapies
  • Peptides
  • Polymers

Leading Sponsors Covered

  • Lipocine Inc.
  • Nanjing Minova Pharmaceutical Co., Ltd.
  • Hansoh Pharmaceutical Co., Ltd.
  • DuKang Pharmaceuticals, Inc.
  • Chengdu Kanghong Pharmaceutical Group Co., Ltd.
  • Biogen
  • Supernus Pharmaceuticals, Inc.
  • Reunion Neuroscience Inc.
  • Bristol-Myers Squibb
  • Brii Biosciences Limited

Geographies Covered

  • North America
  • Europe
  • Asia Pacific
  • Others

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