Viewing Study NCT03823118


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Study NCT ID: NCT03823118
Status: COMPLETED
Last Update Posted: 2023-02-23
First Post: 2019-01-28
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: S1 Plus Anlotinib in Treating Patients With Refractory or Relapsed Small-cell Lung Cancer
Sponsor: Taizhou Hospital
Organization:

Study Overview

Official Title: S1 Plus Anlotinib in Treating Patients With Refractory or Relapsed Small-cell Lung Cancer:An One-arm, Phase Ⅱ, Multi-center Clinical Study (SALTER TRIAL)
Status: COMPLETED
Status Verified Date: 2023-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the efficacy and safety of S1 combination with Anlotinib in patients with small cell lung cancer whose cancer has progression or recurrence after at least one standard chemotherapy.
Detailed Description: Although SCLC is very responsive to initial treatment, most patients relapse with relatively resistant disease.These patients have a median survival of only 4 to 5 months when treated with further systemic therapy. Improvements in therapy for relapsed SCLC are much needed.The purpose of this study is to assess the efficacy and safety of S1 combination with Anlotinib in patients with small cell lung cancer whose cancer has progression or recurrence after at least one standard chemotherapy.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: