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Shionogi, Inc

🇯🇵Japan
Ownership
-
Established
1919-01-01
Employees
-
Market Cap
$13.1B
Website
https://www.shionogi.com/jp/ja/

Clinical Trials

76

Active:0
Completed:60

Trial Phases

4 Phases

Phase 1:23
Phase 2:22
Phase 3:22
+1 more phases

Drug Approvals

1

EMC:1

Drug Approvals

Mulpleo 3 mg film-coated tablets

Approval Date
Jul 7, 2025
EMC

Clinical Trials

Distribution across different clinical trial phases (72 trials with phase data)• Click on a phase to view related trials

Phase 1
23 (31.9%)
Phase 2
22 (30.6%)
Phase 3
22 (30.6%)
Not Applicable
5 (6.9%)

A Study of S-892216-PO in Participants With Renal Impairment and Matched Controls

Not Applicable
Recruiting
Conditions
Renal Impairment
Interventions
Drug: S-892216-PO
First Posted Date
2025-10-17
Last Posted Date
2025-10-30
Lead Sponsor
Shionogi
Target Recruit Count
40
Registration Number
NCT07217886
Locations
🇺🇸

Orlando Clicinal Research Center, Orlando, Florida, United States

🇺🇸

Global Clinical Professionals (GCP) LLC, St. Petersburg, Florida, United States

🇺🇸

Genesis Clinical Research, Tampa, Florida, United States

and more 1 locations

A Study of S-337395 in Symptomatic Nonhospitalized Adults With Respiratory Syncytial Virus (RSV) Who Are at High Risk of Progression to Severe Disease

Not Applicable
Not yet recruiting
Conditions
Respiratory Syncytial Virus Infections
Interventions
Drug: Placebo
First Posted Date
2025-10-09
Last Posted Date
2025-10-09
Lead Sponsor
Shionogi
Target Recruit Count
192
Registration Number
NCT07214571

Study of S-606001 as an Add-on to Enzyme Replacement Therapy (ERT) in Participants With Late-onset Pompe Disease (LOPD)

Not Applicable
Not yet recruiting
Conditions
Pompe Disease
Interventions
Drug: Placebo
First Posted Date
2025-08-14
Last Posted Date
2025-10-16
Lead Sponsor
Shionogi
Target Recruit Count
45
Registration Number
NCT07123155
Locations
🇺🇸

University of California - Irvine Medical Center, Irvine, California, United States

🇺🇸

University of Florida (UF) - Gainesville, Gainesville, Florida, United States

🇺🇸

Emory University Hospital, Atlanta, Georgia, United States

and more 25 locations

Study of S-892216 Long-acting Injectable (LAI) in Healthy Adult Participants

Not Applicable
Recruiting
Conditions
Healthy Participants
Interventions
Drug: S-892216-LAI
Drug: Placebo
First Posted Date
2025-07-30
Last Posted Date
2025-08-27
Lead Sponsor
Shionogi
Target Recruit Count
98
Registration Number
NCT07093580
Locations
🇺🇸

ICON Clinical Research: Lenexa, Lenexa, Kansas, United States

🇺🇸

ICON Clinical Research: Salt Lake City, Salt Lake City, Utah, United States

Phase 1 Study of BPN14770 in Participants With Hepatic Impairment and Healthy Controls

Phase 1
Recruiting
Conditions
Hepatic Impairment
Interventions
First Posted Date
2025-06-12
Last Posted Date
2025-09-05
Lead Sponsor
Shionogi
Target Recruit Count
32
Registration Number
NCT07018492
Locations
🇺🇸

Texas Liver Institute, San Antonio, Texas, United States

🇺🇸

Division of Clinical Pharmacology, University of Miami, Miami, Florida, United States

🇺🇸

Orlando Clinical Research Center, Orlando, Florida, United States

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News

Shionogi's Cefiderocol Shows Superior Outcomes When Used as Early Treatment for Drug-Resistant Infections

Real-world data from the PROVE study demonstrates that cefiderocol achieved a 73.7% clinical cure rate when used as empiric treatment compared to 54.3% when used as salvage therapy for serious gram-negative bacterial infections.

Dovato Demonstrates Non-Inferior Efficacy to Biktarvy with Significantly Less Weight Gain in 96-Week HIV Treatment Study

ViiV Healthcare's PASO DOBLE trial shows Dovato (DTG/3TC) maintains viral suppression as effectively as Biktarvy (BIC/FTC/TAF) at 96 weeks in 553 virologically suppressed HIV-1 patients.

Early Long COVID Trials of Paxlovid and Monoclonal Antibodies Show No Significant Benefits, But Research Continues

Three prominent clinical trials testing Paxlovid and monoclonal antibodies for Long COVID failed to show significant health improvements compared to placebo groups.

ViiV Healthcare Expands Generic License for Long-Acting HIV Treatment to 133 Countries

ViiV Healthcare has expanded its voluntary licensing agreement with the Medicines Patent Pool to allow generic production of cabotegravir for HIV treatment in 133 countries, including all low-income and Sub-Saharan African nations.

ViiV Healthcare Presents Real-World Data on Long-Acting HIV Treatments at IAS 2025

ViiV Healthcare presented extensive real-world data at IAS 2025 demonstrating the effectiveness, safety, and tolerability of its long-acting injectable HIV treatments, including cabotegravir + rilpivirine LA for treatment and cabotegravir LA for prevention.

Stallergenes Greer Transitions Actair® Promotional Activities from Shionogi to CEOLIA in Japan

Stallergenes Greer has appointed CEOLIA Pharma as its new promotional partner for Actair® in Japan, ending a 15-year licensing agreement with Shionogi that began in 2010.

BioVersys and Shionogi Form Strategic Partnership to Develop Novel NTM Treatments Worth Up to CHF 484 Million

BioVersys and Shionogi have entered a research collaboration and exclusive license option agreement to develop novel ansamycin leads from BioVersys' BV500 program targeting non-tuberculous mycobacteria infections.

Shionogi and Cilcare Partner in €400M Deal to Develop Novel Hearing Loss Treatments

Shionogi has entered into a joint research agreement with Cilcare to develop innovative treatments for hearing loss, a condition affecting 5% of the global population with no effective treatments currently available.

Shionogi to Acquire Japan Tobacco's Pharma Units for $1.1 Billion

Japanese pharmaceutical company Shionogi has announced a $1.1 billion acquisition of Torii Pharmaceutical and other pharmaceutical assets from Japan Tobacco, marking a significant consolidation in the Japanese pharma sector.

F2G's Novel Antifungal Olorofim Shows Promise Despite FDA Setback, Phase 2b Results Published in The Lancet

F2G's olorofim, the first in a new class of orotomide antifungals, received a complete response letter from the FDA requiring additional data before approval.

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