Phase 1/2A Study of OTP-01, a Dual Paratopic PD-1/VEGFR2 Antibody, in Patients With Advanced Solid Tumors

Ottimo Pharma Limited12 个研究点分布在 3 个国家目标入组 170 人开始时间: 2025年12月17日最近更新: 2026年4月16日

干预措施OTP-01

概览

阶段: 1 期
状态: 招募中
发起方: Ottimo Pharma Limited
入组人数: 170
试验地点: 12
主要终点: Phase 1 and Phase 2A: Frequency and Severity of adverse events (AEs) and serious adverse events (SAEs)

概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

概览

简要总结

The main goals of this clinical trial are to find out what the best dose of the study drug, OTP-01, is for patients with solid tumors through understanding how it is tolerated and any side effects that it may cause. The trial will also see if OTP-01 causes tumors to shrink and how the body processes OTP-01 by measuring drug levels in the blood.

The main questions this study aims to answer are:

What is the recommended dose of OTP-01 for adults with solid tumors?
Is OTP-01 safe and tolerable?
Does OTP-01 reduce tumor growth?

Participants will:

Receive OTP-01 through an infusion into a vein. Doses will be spaced out and never more than once a week.
Have blood tests to evaluate safety and drug levels of OTP-01. These will be done often at first and then less frequently as treatment continues.
Have radiographic scans of their tumor at baseline and during the study at regular intervals.
Have the choice to have an optional tumor biopsy before and after treatment to help researchers understand how OTP-01 affects cancer and the immune system. These biopsies are voluntary and will not affect participation in the study.

研究设计

研究类型: Interventional
分配方式: Non Randomized
干预模型: Sequential
主要目的: Other
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Histologically or cytologically confirmed advanced (incurable, recurrent, unresectable, or metastatic) solid tumors.
•For dose escalation cohort patients: patients must have a tumor type as defined in the protocol. Patients will have progression on or after or intolerance to most recent systemic therapy. Patients must have received approved standard therapy that is available to the patient that is known to confer clinical benefit, unless this therapy is contraindicated, intolerable to the patient, or is declined by the patient. The reason for treatment decline must be clearly documented in the medical record.
•For backfill cohorts: patients must have a tumor type as defined in the protocol. If patients decline an available standard therapeutic regimen known to confer benefit to enroll on this study, the discussion must be clearly documented in the medical record.
•Measurable disease per RECIST v1.
•Additionally, patients with breast or ovarian cancer with non-measurable, evaluable disease are eligible.
•ECOG performance status 0-
•Life expectancy of at least 3 months.
•Willing to provide a pretreatment tumor sample (either an archival sample or a sample obtained by pretreatment biopsy).
•All toxicity resulting from prior cancer therapies must have resolved to NCI CTCAE v5.0 ≤ Grade 1 or pre-therapy baseline with the exception of alopecia or ≤ Grade 2 neuropathy.
•Adequate hematological, renal, and hepatic function.

排除标准

•Receiving systemic corticosteroids at prednisone-equivalent dose of \> 10 mg/day within 4 weeks prior to signing consent. Chronic systemic corticosteroid therapy for physiologic replacement (≤ 10 mg/day of prednisone equivalents) and the use of non-systemic corticosteroids (e.g., inhaled, topical, intra-nasal, intra-articular, or ophthalmic) are permitted
•History of Grade 4 allergic or anaphylactic reaction to prior monoclonal antibody therapy or allergic reaction to any excipients within the investigational product
•History of toxicity requiring permanent discontinuation of prior cancer immunotherapy
•Have an active autoimmune disease that has required systemic treatment in past 2 years (replacement therapy is not considered a form of systemic treatment)
•History of organ or stem cell transplant or need for immunosuppressive treatment
•Have proteinuria \> 2 + (within 7 days prior to initiation of study treatment).
•Received any chemotherapy, immunotherapy or investigational anticancer therapy within 3 weeks or 5 half-lives (whichever is shorter; minimum of 2 weeks) prior to first dose of study drug
•Definitive radiotherapy within 6 weeks and palliative radiation within 2 weeks prior to the first dose of study drug. If previously irradiated, lesions must have demonstrated clear-cut progression prior to being eligible for evaluation as target lesions
•Other protocol and subprotocol-defined exclusion criteria apply

研究组 & 干预措施

Monotherapy Dose Escalation with Backfill

Experimental

干预措施: OTP-01 (Drug)

Monotherapy Dose Expansion

Experimental

干预措施: OTP-01 (Drug)

结局指标

主要结局

Phase 1 and Phase 2A: Frequency and Severity of adverse events (AEs) and serious adverse events (SAEs)