[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

Find a Study Site

Study’s contact

Call center

+86 21 6882 1388

Email address

GFH925X0201@genfleet.com

Condition

Advance Non-small Cell Lung Cancer

Treatment type

Interventional

Investigational product

Cetuximab

Phase

Phase 1/Phase 2

Sponsor

Genfleet Therapeutics (Shanghai) Inc.

ClinicalTrials.gov identifier

NCT05756153

Study number

GFH925X0201

Understanding clinical trials

Get answers to your questions about clinical trials.

About the study

This is a Phase Ib/II study. The objectives are to evaluate the safety/tolerability and efficacy of GFH925 in combination with Cetuximab in advanced KRAS G12C mutant NSCLC, to characterize pharmacokinetics (PK) of GFH925 in combination with Cetuximab in advanced KRAS G12C mutant NSCLC

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Patient has provided informed consent form (ICF).
  2. Males or females aged ≥ 18 years.
  3. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0~1.
  4. Life expectancy > 3 months judged by the investigator.
  5. Have histologically or cytologically confirmed advanced KRAS G12C-mutated NSCLC.
  6. Have at least one measurable lesion per RECIST 1.1.
  7. Have sufficient organ functions.
  8. With toxicities left from prior anti-tumor therapy resolved to baseline or CTCAE Grade 1 (neurotoxicity or alopecia ≤ Grade 2).
  9. Women of childbearing potential (WOCBP) and male patients with WOCBP partners must agree to use effective contraception method during the study specified period.
Exclusion criteria

  1. With clinically significant cardiovascular diseases.
  2. With active central nervous system (CNS) metastases and/or carcinomatous meningitis.
  3. With clinically significant gastrointestinal diseases.
  4. With active infections.
  5. With uncontrollable or symptomatic pleural effusion, ascites, or pericardial effusion.
  6. With uncontrolled systemic diseases, such as hypertension or diabetes.
  7. Prior treatment with an inhibitor specific to KRAS G12C.
  8. Major surgery within 4 weeks prior to initiation of study treatment.
  9. With known allergies to the study drugs or components.
  10. Pregnant or lactating females, or female patients intend to become pregnant during participation.

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

Find a Study Site