A Clinical Study of SHR-4506 Injection in Patients With Malignant Tumors

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorSuzhou Suncadia Biopharmaceuticals Co., Ltd.

About this trial

The study is being conducted to evaluate the safety and tolerability of SHR-4506 Injection in patients with malignant tumors and to determine the maximum tolerated dose (MTD) or maximum administered dose (MAD).

Eligibility criteria

Qualifiers

Age ≥18 years, any gender.

ECOG performance status 0-1.

Histologically or cytologically confirmed malignant tumor patients who have failed standard therapy, or are intolerant to standard therapy, or have no standard treatment available.

Adequate organ function.

Disqualifiers

Prior treatment with the same class of investigational drug.

Confirmed or suspected central nervous system (CNS) tumor involvement.

Uncontrolled tumor-related pain.

Active autoimmune disease, history of immunodeficiency (including primary or secondary, e.g., HIV infection), or autoimmune disorders requiring systemic therapy.

Trial design

Treatments tested in this trial

  • SHR-4506 Injection

Treatment groups

102 Participants
are divided into 1 treatment group