Evaluation of ICP-B208 in Patients With Advanced Solid Tumors

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorBeijing InnoCare Pharma Tech Co., Ltd.

About this trial

To evaluate the safety, tolerability, efficacy and pharmacokinetic characteristics of ICP-B208 in the trial participants of unresectable advanced or metastatic solid tumors

Eligibility criteria

Qualifiers

18 years old to 75 years old;

Unresectable locally advanced or metastatic gastrointestinal tumors or other advanced solid tumors that have failed previous systemic treatment and have been confirmed by histopathology or cytology;

The ECOG physical fitness score is 0 to 1 point.

There is at least one measurable lesion;

Disqualifiers

Other active malignant tumors occurred within 3 years before the first administration of the study drug;

Received the anti-tumor treatment defined by the protocol within the time range before the first administration of the study drug specified in the protocol;

Trial participants with unstable primary CNS tumors or CNS metastases;

Uncontrollable or significant major cardiovascular diseases;

Trial design

Treatments tested in this trial

  • ICP-B208

Treatment groups

539 Participants
are divided into 1 treatment group