Testing IBI3009 in adults with advanced small cell lung cancer
Tests IBI3009, a new drug, in adults with advanced small cell lung cancer.
Plain-language title generated from the registry record
Registry title: Study of IBI3009 in Participants with Unresectable, Metastatic or Extensive-Stage Small Cell Lung Cancer
Key facts
- Where
- Heidelberg, Westmead, and Wollongong, AustraliaSee the 3 sites
- Phase
- Phase 1
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with small cell lung cancer that cannot be removed by surgery, has spread, or is at the extensive stage. It tests the safety of IBI3009.
- Age
- 18 years or older. In Part 1 of the trial, 18 to 75 years.
- Sex
- Men and women can join.
- Disease stage
- Small cell lung cancer, confirmed by tissue or cell tests, that cannot be removed by surgery, has spread (metastatic), or is extensive-stage.
- Earlier treatment
- Side effects from earlier cancer treatment must have gone away or be mild (Grade 0 or 1), apart from things like hair loss or tiredness.
Main reasons for not taking part
- Taking part in another interventional clinical study
- Known allergy or intolerance to IBI3009 or its ingredients
- Major surgery in the 4 weeks before the first dose, or severe unhealed wounds
- Pregnant, positive pregnancy test, or breastfeeding
- Not fit to join in the investigator's judgement
Read by machine on 12 November 2026.
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 75 years old?
Source: NCT06613009, who can take part
Where in Australia
- Austin HospitalHeidelberg, AustraliaContact: Lue ShenTaking people
- Westmead HospitalWestmead, AustraliaContact: Pei DingTaking people
- Wollongong HospitalWollongong, AustraliaContact: Lue ShenNot yet recruiting
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Innovent Biologics (Suzhou) Co. Ltd.
- Trial code
- NCT06613009EU 2025-523972-21-00
- Record updated
- 11 February 2025
- Original description
The main purpose of this study is to evaluate the safety and tolerability of IBI3009 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RDE) of IBI3009.Read full original descriptionShow less
A Phase 1 Multicenter, Open-label Study of IBI3009 in Participants with Unresectable, Metastatic or Extensive-Stage Small Cell Lung Cancer
The main purpose of this study is to evaluate the safety and tolerability of IBI3009 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RDE) of IBI3009.
Inclusion: Participants have the ability to understand and give written informed consent for participation in this trial, including all evaluations and procedures as specified by this protocol; Male or female subjects ≥ 18 years old. For Part 1, age ≥18 years and ≤75 years; Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0-1; Minimum life expectancy of ≥ 12 weeks; Adequate organ function confirmed at screening period; Histologically or cytologically confirmed unresectable,metastatic or Extensive-Stage small cell lung cancer (SCLC).
Exclusion: Has adverse reactions resulting from previous anti-tumor therapies, which have not resolved to Grade 0 or 1 toxicity according to NCI CTCAE v5.0 (except for alopecia, fatigue, pigmentation and other conditions with no safety risk according to investigator's discretion) prior to the first dose of the study drug; Undergone major surgery (Craniotomy, thoracotomy or laparotomy, and other surgery according to investigator's discretion, excluding needle biopsy) within 4 weeks prior to the first dose of the study drug, or who are expected to undergo major surgery during the study period, or who have severe unhealed wounds, trauma, ulcers, etc; Known allergies, hypersensitivity, or intolerance to IBI3009 or its excipients; Participating in any other interventional clinical research except observational (non-interventional) study or in the follow-up phase of an interventional study; Women who are pregnant, have positive results in pregnancy test or are lactating; Not eligible to participate in this study at the discretion of the investigator.