New drug SKB410 enters human testing for Hard-to-Treat cancers
NCT ID NCT05906537
First seen Jun 27, 2026 · Last updated Aug 05, 2026 · Updated 2 times
Summary
This early-stage study tests a new drug called SKB410 in about 54 adults with advanced solid tumors who have no standard treatment options left. The main goals are to check the drug's safety, find the best dose, and see if it can shrink tumors. Participants receive multiple doses and are closely monitored for side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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38 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Mar 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. At the time of signing the ICF: age ≥ 18 years, male or female. 2. Subjects with histologically or cytologically confirmed locally advanced or metastatic solid tumors who have failed/are intolerant/ineligible to or do not have standard therapy, and have at least one measurable lesion meeting Response Evaluation Criteria in Solid Tumors (RECIST v1.1). 3. Eastern Cooperative Oncology Group (ECOG) score of 0 to 1. 4. Expected survival ≥ 3 months. 5. Subjects with adequate organ and bone marrow function confirmed by laboratory results within 3 days prior to the first dose. 6. Subjects of childbearing potential (male or female) must use effective medical contraception during the study and continue contraception until 210 days after the last dose for female subjects and until 120 days after the last dose for male subjects. 7. Ability to understand and willingness to sign ICF, and will be able to comply with the protocol-specified visits and relevant procedures. Exclusion Criteria: 1. Has received anti-tumor therapy, including chemotherapy, targeted therapy, tumor immunotherapy, and traditional Chinese medicinal products with anti-tumor indications, within 4 weeks prior to the first dose or within 5 half-lives of known drugs (whichever is shorter). 2. Has received radiotherapy within 4 weeks prior to the first dose. 3. Has had major surgery within 4 weeks prior to the first dose. 4. Has received strong cytochrome P450 (CYP3A4) inhibitors or inducers (see Annex 4) within 2 weeks prior to the first dose or within 5 half-lives of known drug, whichever is longer. 5. Has not recovered to normal or ≤ Grade 1 from any AE and/or complication due to any prior therapy (except alopecia or pigmentation). 6. Has known history of allergy to any component of SKB410 or other monoclonal antibodies. 7. Has a known previous or concurrent other malignancies within 5 years prior to signing the ICF. 8. Presence of active central nervous system (CNS) metastases and/or carcinomatous meningitis. 9. Has active autoimmune disease with systemic therapy or immunosuppressive therapy within 2 years prior to signing the ICF. 10. Has uncontrolled or severe cardiovascular disease. 11. Has uncontrolled systemic diseases. 12. Presence of clear neurological or psychiatric disorder. 13. Has active infection requiring systemic. 14. Has human immunodeficiency virus (HIV) infection; has any active viral hepatitis. 15. Pregnant or lactating. 16. Has prior autologous/allogeneic hematopoietic stem cell transplantation or solid organ transplantation. 17. Has any other conditions such as medical history, treatment and laboratory abnormalities that may confound the study results, interfere with the subject's compliance, or impair the subject's interests, as assessed by the investigator or the sponsor.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Beijing Cancer Hospital
Beijing, Beijing Municipality, 100142, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Mitochondria-Targeting drug gamitrinib tested for first time in humans
- Can a Two-Drug combo outsmart advanced cancer?
- Can an experimental pill boost cancer immunotherapy? early trial puts HG146 to the test
- New injectable drug tested for safety in Hard-to-Treat solid tumors
- New antibody drug conjugate tested against advanced cancers