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NCT06985368

A Clinical Trial of SIBP-A18 Injection in the Treatment of Advanced Malignant Solid Tumor Patients

Recruiting now Phase 1 Last updated 7 January 2026
What this trial tests

Phase 1 trial testing SIBP-A18 in Solid Tumor Malignancy in 156 participants. Currently enrolling.

Timeline
16 June 2025
Primary endpoint
15 May 2028
15 September 2028

Quick facts

Lead sponsorShanghai Institute Of Biological Products
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment156
Start date16 June 2025
Primary completion15 May 2028
Estimated completion15 September 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Institute Of Biological Products

Who can join

Adults 18 to 75, any sex, with Solid Tumor Malignancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main purpose To evaluate the safety, tolerability, and pharmacokinetic characteristics of SIBP-A18 and determine the maximum tolerable dose (MTD) and phase II recommended dose (RP2D). A secondary purpose To preliminarily evaluate the anti-tumor efficacy of SIBP-A18. Evaluate the effect of SIBP-A18 injection on Q to T interval/Corrected QT interval (QT/QTc interval) in participants with advanced solid tumors

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Solid Tumor Malignancy

Currently open trials in the same condition.

Other Shanghai Institute Of Biological Products trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06985368.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing