SC-002 in Small Cell Lung Cancer and Large Cell Neuroendocrine Carcinoma
Status: | Terminated |
---|---|
Conditions: | Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/7/2018 |
Start Date: | June 2015 |
End Date: | August 23, 2018 |
A Phase 1a/1b Dose Escalation and Expansion Study of Single-agent SC-002 in Subjects With Relapsed or Refractory Small Cell Lung Cancer and Large Cell Neuroendocrine Carcinoma
This is a Phase 1a/1b study of SC-002 in patients with relapsed small cell lung cancer (SCLC)
or large cell neuroendocrine carcinoma (LCNEC). SC-002 is an antibody-drug conjugate (ADC)
comprised of a monoclonal antibody linked to a potent chemotherapy.
The purpose of this study is to assess the safety and tolerability of SC-002 at different
dose levels, to determine the highest dose of SC-002 that can be given to patients with SCLC
or LCNEC, to evaluate the side effects of SC-002, and to assess the anti-cancer activity of
SC-002.
or large cell neuroendocrine carcinoma (LCNEC). SC-002 is an antibody-drug conjugate (ADC)
comprised of a monoclonal antibody linked to a potent chemotherapy.
The purpose of this study is to assess the safety and tolerability of SC-002 at different
dose levels, to determine the highest dose of SC-002 that can be given to patients with SCLC
or LCNEC, to evaluate the side effects of SC-002, and to assess the anti-cancer activity of
SC-002.
Part 1A is a dose escalation study in patients with small cell lung cancer or large cell
neuroendocrine carcinoma with cytologically confirmed, limited or extensive SCLC or LCNEC
that have relapsed or refractory limited or extensive disease following no more than 2 prior
chemotherapy regimens.
Part 1B is an expansion study where patients will be enrolled and treated in order to further
characterize safety and preliminary efficacy in patients with SCLC or LCNEC and further
characterize PK, immunogenicity and target expression and possible relationship to clinical
outcome.
neuroendocrine carcinoma with cytologically confirmed, limited or extensive SCLC or LCNEC
that have relapsed or refractory limited or extensive disease following no more than 2 prior
chemotherapy regimens.
Part 1B is an expansion study where patients will be enrolled and treated in order to further
characterize safety and preliminary efficacy in patients with SCLC or LCNEC and further
characterize PK, immunogenicity and target expression and possible relationship to clinical
outcome.
Inclusion Criteria:
- Histologically or cytologically confirmed SCLC (either limited or extensive disease)
or LCNEC, that has relapsed from the most current treatment or was refractory to
treatment
- Evidence of progressive disease during or following no more than 2 prior chemotherapy
regimens
- Measurable disease as defined by RECIST
- ECOG performance status of 0 or 1
- Adequate hematological and organ function as confirmed by laboratory values
- Treatment with anticancer/investigational drugs, therapy ≤ 4 weeks prior to first dose
of SC-002
Exclusion Criteria:
- Active central nervous system metastases
- Uncontrolled cardiac disease
- Positive serology for hepatitis B or hepatitis C or known HIV infection
- Presence of any condition that may increase the risks associated with study
participation and interfere with the interpretation of study results
We found this trial at
4
sites
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