Recruiting
Phase 1

IFx-Hu2.0 & Pembrolizumab

Sponsor:

TuHURA Biosciences, Inc.

Code:

NCT06940440

Conditions

Advanced Or Metastatic Merkel Cell Carcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

IFx-Hu2.0

Pembrolizumab

Study Details

Brief summary:

This Phase 1, multicenter, open-label trial will assess the safety and feasibility of IFx-Hu2.0 as adjunctive therapy to pembrolizumab in adult participant (≥18 years) with non-cutaneous Merkel Cell Carcinoma. Nine participants will receive IFx-Hu2.0 as a visceral/nodal lesion injection followed by pembrolizumab.

Conditions

Advanced Or Metastatic Merkel Cell Carcinoma

Study ID

NCT06940440

Start date

Jan 27, 2026

Status verified date

Oct, 2026

Completion date

May 31, 2028

Anticipated

Primary completion date

Apr, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. At least 18 years of age.
2. Life expectancy equal to or greater than six months.
3. Eastern Cooperative Oncology Group (ECOG) Performance Status < 2.
4. Has measurable disease as defined by RECIST v1.1
5. Must be recurrent and/or unresectable Stage III or Stage IV American Joint Committee on Cancer (AJCC) (8th edition) and have histologically confirmed advanced or metastatic Merkel cell carcinoma

a. Must have at least one deep-seated visceral/nodal greater than 3 mm in its longest diameter
6. Subject should be CPI naïve i.e., no prior therapy with CPI including but not limited to Pembrolizumab, avelumab, ipilimumab, nivolumab.
7. Tumor tissue from an archival core biopsy or resected site of disease must be provided for biomarker analyses. If archival tissue is not available, then a new biopsy should be performed.
8. Adequate hematological, hepatic, and renal function according to laboratory ranges and medical criteria defined within the study protocol.

Exclusion Criteria

1. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with protocol requirements.
2. Subjects with active brain metastases, with the exception of treated brain metastases that have imaging proving stability at least 4 weeks after treatment, no new metastases, and not requiring steroids.
3. Subjects with recurrent resectable MCC
4. Subjects who have received prior systemic chemotherapy
5. Pregnant or breastfeeding females and females desiring to become pregnant or breastfeed within the timeframe of this study.
6. Active, known, or suspected autoimmune disease. Potential subjects with type I diabetes mellitus, residual hypothyroidism due to autoimmune thyroiditis only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment are permitted to enroll. Low grade autoimmune toxicity is NOT an exclusion under this criterion.
7. A condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of IFx-Hu2.0 administration. Inhaled or topical steroids are permitted in the absence of active autoimmune disease.

Study Design

Enrollment

9 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: IFx-Hu2.0

Participants will receive IFx-Hu2.0 0.1 mg as a visceral/nodal lesion injection in a single lesion once per week for 3 consecutive weeks. At the discretion of the investigator, the same lesion will be injected at each injection visit, unless the initially injected lesion is no longer suitable for injection; alternatively, another lesion may be injected if the participant has other visceral/nodal lesions that meet the protocol injection criteria and are considered safe to inject. Pembrolizumab (200 mg) will be administered IV at Visit 1 (within 48 hours after the first IFx-Hu2.0 injection) and then every 3 weeks for approximately 6 months until disease progression or unacceptable immune-related toxicity.

Interventions

IFx-Hu2.0

Therapeutic Classification:

• Innate immune agonist

Route of Administration:

• Intralesional

Pembrolizumab

Therapeutic Classification:

• Immunotherapy (Immune checkpointinhibitor)

Route of administration:

• Intravenous (IV) infusion

Primary outcome measure

  • Safety [ Time Frame: 28 days from last dose of IFx-Hu2.0 ]
  • Feasibility [ Time Frame: 28 days from last dose of IFx-Hu2.0 ]

Central Contacts and Locations

Central contacts

Locations

H. Lee Moffitt Cancer Center and Research Institute

Recruiting

Tampa, Florida, United States, 33612

Contacts

Principal Investigator:

Andrew S Brohl, MD

University of Wisconsin Carbone Cancer Center

Recruiting

Madison, Wisconsin, United States, 53792

Contacts

Principal Investigator:

Ma Vincent, MD

More Information

Sponsor

TuHURA Biosciences, Inc.

Last update posted

Oct 21, 2026

Last verified

Oct, 2026

Keywords

  • Metastatic
  • Advanced
  • Merkel Cell Carcinoma

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-25. This information was provided to ClinicalTrials.gov by TuHURA Biosciences, Inc. on 2026-10-21. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.