Tecovirimat for Treatment of Monkeypox Virus - Study Extension Providing Standard of Care Only

NCT ID: NCT06721585

Last Updated: 2025-09-04

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 328 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-07-10
• Study Completion Date: 2025-08-30

Brief Summary

The purpose of the PALM007 extension is to further characterize the clinical and natural history of mpox, and to provide standard of care (SOC) during the ongoing outbreaks.

Detailed Description

This open-label extension to the PALM007 protocol began in July 2024 after enrollment into the main study ended. It will further clinically characterize the natural history of mpox, and continue to identify recrudescent cases. Participants were initially provided SOC as well as open-access tecovirimat. The results of PALM007 were unblinded in August 2024, and although no safety concerns were observed with tecovirimat use, efficacy, defined by improvement in days to complete mpox skin lesion resolution, was not observed for tecovirimat compared to placebo. Therefore, the administration of tecovirimat in the extension amendment was discontinued in early August 2024, once these results were known, and only SOC continues to be provided.

Participants are admitted to the hospital and receive SOC for mpox until they have recovered. Recovery is defined as resolution of all lesions and a negative blood test for MPXV. Participants will remain on study through day 59 but will not have a scheduled study visit unless they present with new mpox symptoms. Sick visits will be available for participants who reach full body lesion resolution but subsequently develop at least 1 new lesion consistent with mpox after discharge and on or before day 59, at which time viral PCR and clinical laboratory testing will be performed and participants will be offered standard of care.

Initially, all participants presenting with mpox were eligible to enroll in this extension, regardless of disease severity. As of 05May2025, only patients with severe disease, defined as the presence of any of the following: flat lesions, pregnancy (due to risk for serious complications), suspected sickle cell disease, or severe clinical disease will be enrolled.

Conditions

Mpox (Monkeypox)

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Open-access tecovirimat plus SOC for mpox

Participants are provided SOC as well as open-access tecovirimat. Tecovirimat capsules are administered orally to participants for 14 days based on participant weight.

Closed to new participants in August 2024.

Tecovirimat Oral Capsule [Tpoxx]

Intervention Type: DRUG

Tecovirimat Oral Capsule 200 mg capsules

Number of capsules and frequency of dosage will be based on participant weight:

• ≥120 kg: three capsules three times a day (total daily tecovirimat dose: 1,800 mg)
• 40 to <120 kg: three capsules twice a day (total daily tecovirimat dose: 1,200 mg)
• 25 to <40 kg: two capsules twice a day (total daily tecovirimat dose: 800 mg)
• 13 to <25 kg: one capsule twice a day (total daily tecovirimat dose: 400 mg)
• 6 to <13 kg: ½ the contents of a capsule twice daily (total daily tecovirimat dose: 200 mg)
• 3 to <6 kg: ¼ the contents of a capsule twice daily (total daily tecovirimat dose: 100 mg)

Standard of Care (SOC)

Intervention Type: OTHER

Participants are provided SOC for mpox

Standard of care for mpox

Participants are provided SOC for mpox.

Standard of Care (SOC)

Intervention Type: OTHER

Participants are provided SOC for mpox

Interventions

Tecovirimat Oral Capsule [Tpoxx]

Tecovirimat Oral Capsule 200 mg capsules

Number of capsules and frequency of dosage will be based on participant weight:

• ≥120 kg: three capsules three times a day (total daily tecovirimat dose: 1,800 mg)
• 40 to <120 kg: three capsules twice a day (total daily tecovirimat dose: 1,200 mg)
• 25 to <40 kg: two capsules twice a day (total daily tecovirimat dose: 800 mg)
• 13 to <25 kg: one capsule twice a day (total daily tecovirimat dose: 400 mg)
• 6 to <13 kg: ½ the contents of a capsule twice daily (total daily tecovirimat dose: 200 mg)
• 3 to <6 kg: ¼ the contents of a capsule twice daily (total daily tecovirimat dose: 100 mg)

Intervention Type: DRUG

Standard of Care (SOC)

Participants are provided SOC for mpox

Intervention Type: OTHER

Other Intervention Names

TPOXX

Eligibility Criteria

Inclusion Criteria

1. Laboratory-confirmed mpox infection as determined by PCR obtained from blood, oropharynx, or skin lesion within 48 hours of screening

2. Mpox illness of any duration provided that the patient has at least one active, not yet scabbed, lesion

3. Stated willingness to comply with all study procedures (including required inpatient stay) and availability for the duration of the study

4. Ability to provide informed consent personally or by a legally or culturally acceptable representative if the patient is unable to do so

5. Severe disease, defined as the presence of at least one of the following:

1. Flat lesions (flat and soft lesions; no pustules or vesicles visible to the eye)

2. Pregnancy (due to risk of serious complication)

3. Suspected sickle cell disease

4. Severe clinical disease, defined as having at least 3 of the following:

• Lesion count greater than 250
• Fever for greater than 48 hours
• Hypotension (systolic blood pressure less than 90 mmHg or diastolic blood pressure less than 60 mmHg)
• Pallor
• Respiratory distress
• Altered mental status
• Extreme lethargy
• Painful oral lesions making oral intake difficult
• Difficulty peeing or pooping due to painful lesions
• Painful lesions on hands and feet
• Tachycardia (heart rate greater than 100 beats per minute)
• Diarrhea (greater than or equal to 3 liquid stools per 24 hours)

Exclusion Criteria

1. Severe anemia, defined as hemoglobin less than 7 g/dL

2. Current or planned use of another investigational drug at any point during study participation

3. Patients who, in the judgement of the investigator, will be at significantly increased risk as a result of participation in the study

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Institut National de Recherche Biomédicale. Kinshasa, République Démocratique du Congo

OTHER

Sponsor Role: collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jean-Jacques Muyembe-Tamfum, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Kinshasa University

Locations

L'Hôpital Général de Référence de Kole

Kole, , Democratic Republic of the Congo

L'Hôpital Général de Référence de Tunda

Tunda, , Democratic Republic of the Congo

Countries

Democratic Republic of the Congo

Provided Documents

Document Type: Informed Consent Form

View Document

Related Links

https://clinicaltrials.gov/study/NCT05559099

PALM 007 Record NCT05559099

Other Identifiers

PALM007-Ext

Identifier Type: -

Identifier Source: org_study_id