Ozmosi | Bemnifosbuvir Drug Profile
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Bemnifosbuvir

Pronounced as: bem-ni-FOS-byu-vir

Alternative Names: Bemnifosbuvir, at-527, at527, at 527, ro7496998, BEM + Ruzasvir, Ruzasvir + BEM
Clinical Status: Active
Latest Update: 2026-04-13
Latest Update Note: Clinical Trial Update

Product Description

Hoffmann-La Roche is developing at-527, an Oral HCV-NS5B Inhibitor for Mild or Moderate COVID-19. (Sourced from: https://forpatients.roche.com/en/trials/infectious-diseases/covid-19-pneumonia/study-to-evaluate-the-effects-of-at-527-in-non-hospital-29576.html)

Mechanisms of Action: HCV-NS5B Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Fast Track - COVID-19 *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Atea
Company Location: Eastern America
Company Founding Year: 2012
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Bemnifosbuvir

Countries in Clinic: Argentina, Brazil, Canada, France, Germany, Greece, India, Japan, Korea, Latvia, Malaysia, Mauritius, Mexico, Moldova, Netherlands, Pakistan, Philippines, Poland, Romania, South Africa, South Korea, Spain, Sweden, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, United States, Unknown Location, Vietnam

Active Clinical Trial Count: 16

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - Atea presented P1 Healthy Volunteers results on 2026-05-29 for Bemnifosbuvir
  • Clinical Outcomes Reported - Atea presented P1 Hepatitis C results on 2026-05-27 for Bemnifosbuvir
  • Clinical Outcomes Reported - Atea presented P2 Hepatitis C results on 2026-05-29 for Bemnifosbuvir

Highest Development Phases

Phase 3: COVID-19|Hepatitis C, Chronic|Severe Acute Respiratory Syndrome

Phase 2: Hepatitis A|Liver Cirrhosis

Phase 1: Healthy Volunteers|Hepatic Insufficiency|Kidney Diseases

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06911320

AT-01B-010

P1

Recruiting

Kidney Diseases|Hepatic Insufficiency

2026-05-01

50%

2026-04-14

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

NCT05904470

AT-01B-004

P2

Completed

Hepatitis C, Chronic|Hepatitis A|Liver Cirrhosis

2024-12-09

41%

2025-02-08

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT06868264

C-BEYOND

P3

Active, not recruiting

Hepatitis C, Chronic

2026-09-01

16%

2025-12-06

Primary Endpoints|Treatments|Trial Status

NCT05629962

SUNRISE-3

P3

Completed

Severe Acute Respiratory Syndrome|COVID-19

2024-04-25

9%

2025-06-14

Patient Enrollment|Primary Endpoints|Treatments

NCT06204679

AT-01B-005

P1

Completed

Healthy Volunteers

2024-08-25

12%

2024-09-20

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT05618314

AT-03A-011

P1

Completed

Kidney Diseases

2024-06-15

50%

2025-08-27

Primary Endpoints|Treatments

NCT06356194

AT-01B-006

P1

Completed

Healthy Volunteers

2024-05-30

12%

2024-08-01

Primary Endpoints|Treatments|Trial Status

NCT05724693

AT-03A-010

P1

Completed

Healthy Volunteers

2024-04-23

12%

2024-08-01

Primary Endpoints

NCT07037277

C-Forward

P3

Recruiting

Hepatitis C, Chronic

2026-12-01

6%

2026-04-14

Primary Endpoints|Start Date|Treatments

2023-504566-28-00

AT-01B-004

P2

Completed

Hepatitis C, Chronic

2025-01-28

2025-05-02

Treatments

jRCT2071240070

jRCT2071240070

P3

Completed

COVID-19

2024-05-30

2023-504540-33-00

AT-03A-017

P3

Completed

COVID-19

2024-05-06

2025-05-02

Treatments

2025-521096-31-00

AT-01B-008

P3

Not yet recruiting

Hepatitis C, Chronic

2027-03-31

NCT07272889

EE/LNG

P1

Completed

Healthy Volunteers

2026-02-17

2026-04-14

Primary Completion Date|Primary Endpoints|Start Date|Study Completion Date|Treatments|Trial Status

NCT06921941

AT-01B-009

P1

Completed

Healthy Volunteers

2025-07-02

50%

2025-08-30

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT07007806

AT-01B-011

P1

Completed

Healthy Volunteers

2025-06-28

50%

2025-08-30

Primary Endpoints|Start Date