Small-cell Lung CancerSUCCEEDNCT06486428
Small Cell Lung Cancer Community Engagement to Eliminate Research Discepancies
An observational study of Small-cell Lung Cancer, run by Addario Lung Cancer Medical Institute at 52 sites in United States.
Trial summary
This study will evaluate if a direct-to-patient, de-centralized, remote approach will improve clinical research outreach and engagement for patients with SCLC, in the context of a bio-specimen collection study. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Small-cell Lung Cancer
- How many people
- 22 participants
- Where
- 52 sitesUnited States
- Study dates
- 23 May 2025to Dec 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adults (USA-based) with a diagnosis of extensive stage primary SCLC or tSCLC
Who may be able to join
- Men or women greater than or equal to 18 years of age at the time of consent
- Ability to read, write and communicate in English
- Provide voluntary consent to participate in this study, documented via a signed informed Consent Form (ICF)
- Willing to provide clinical and medical information related to his/her cancer diagnoses to the study team as required
- Willing to comply with the requirements of the study
- Diagnosis of extensive stage primary SCLC or tSCLC
Who cannot join
- Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements
- Subjects who previously enrolled to this study
- Note: Concurrent enrollment in other clinical trials is NOT exclusionary
Trial locations and contacts
52 sites in 1 country.
52 sites in 1 country
United States52 sites
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Alabama, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Alaska, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Arizona, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Arkansas, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, California, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Colorado, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Connecticut, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Delaware, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, District of Columbia, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Florida, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Georgia, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Hawaii, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Idaho, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Illinois, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Indiana, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Iowa, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Kansas, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Kentucky, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Louisiana, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Maine, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Maryland, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Massachusetts, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Michigan, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Minnesota, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Mississippi, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Missouri, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Montana, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Nebraska, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Nevada, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, New Hampshire, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, New Jersey, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, New Mexico, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, New York, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, North Carolina, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, North Dakota, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Ohio, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Oklahoma, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Oregon, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Pennsylvania, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Rhode Island, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, South Carolina, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, South Dakota, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Tennessee, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Texas, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Utah, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Vermont, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Virginia, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Washington, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, West Virginia, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Wisconsin, 37232
Https://Alcmi.Org/Clinical-Trials/Current-Studies/Succeed-Study.Html
Multiple Locations, Wyoming, 37232
Vanderbilt-Ingram Cancer Center
Nashville, Tennessee, 37232
About this study
Official title: A Study to Evaluate a Remote, Decentralized, Direct-to-Patient Strategy for Clinical Research Engagement of Patients With Small Cell Lung Cancer (SCLC).
This study will evaluate if a direct-to-patient, de-centralized, remote approach will improve clinical research outreach and engagement for patients with SCLC, in the context of a bio-specimen collection study. The study will also assess self-reported preferences and needs of patients with SCLC, regarding choosing and accessing novel therapies in research or standard clinical care settings and supportive gaps in this area, through an initial and 3 month follow up survey.
Read the detailed description
This is a non-interventional, non-treatment, non-randomized, single coordinating center, study to determine the feasibility of decentralized bio-specimen collection in USA-based adult subjects with SCLC, to be conducted in conformance with Good Clinical Practices. Potential study subjects will be referred to contact staff through a dedicated study webpage form or dedicated study phone hotline at the coordinating center (ALCMI) who will handle informed consent, coordinate remote blood sample collection with study subjects, and collect medical records to confirm diagnosis and treatment history. Subjects will also be asked to complete a baseline and follow up questionnaire/survey documenting their self-report diagnosis, treatment history, factors impacting care and quality of life, and needs/preferences regarding supportive resources.
Patients who have been diagnosed with either extensive stage primary SCLC or patients diagnosed with primary NSCLC who experienced histological "transformation" with a SCLC component after initial diagnosis and subsequent treatment (transformed SCLC; tSCLC) will be invited to volunteer for this study.
- Conditions
- Small-cell Lung Cancer
- Keywords
- SCLC, Lung Cancer
- Medical subject headings
- Small Cell Lung Carcinoma, Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| SCLC (primary de novo) | Blood collection, survey (baseline and Month 3) | |
| SCLC (transformed) | Blood collection, survey (baseline and Month 3) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Feasibility of conducting trial in SCLC population
Percentage of overall eligible subjects enrolled. Percentage of primary SCLC eligible subjects enrolled. Percentage of tSCLC eligible subjects enrolled. Percentage of SCLC eligible subjects enrolled compared to percentage of tSCLC eligible subjects enrolled. Percentage of primary SCLC enrolled subjects completed. Percentage of tSCLC enrolled subjects completed. Percentage of SCLC enrolled subjects completed compared to percentage of tSCLC enrolled subjects completed. Overall reasons for early termination. Reasons for early termination from trial in primary SCLC enrolled. Reasons for early termination from trial in tSCLC enrolled.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Jul 2024
- Study start23 May 2025
- Primary completion15 Jul 2026
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Small-cell Lung CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 22 participants (actual)
Sponsor and investigators
- Lead sponsor
- Addario Lung Cancer Medical Institute
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Christine Lovly, MD PhD, Principal investigator, Vanderbilt-Ingram Cancer Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06486428
- Sponsor's protocol ID
- ALCMI-023
- Acronym
- SUCCEED
- Status last verified
- Aug 2026
- First submitted
- 15 Dec 2023
- Last updated
- 4 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Study to Evaluate a Remote, Decentralized, Direct-to-Patient Strategy for Clinical Research Engagement of Patients With Small Cell Lung Cancer (SCLC).
- ClinicalTrials.gov ID
- NCT06486428
- Acronym / sponsor ID
- SUCCEED / ALCMI-023
- Conditions
- Small-cell Lung Cancer
- Keywords
- SCLC, Lung Cancer
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 22 participants (actual)
- Lead sponsor
- Addario Lung Cancer Medical InstituteUniversity, hospital or other
- Study start
- 23 May 2025 (actual)
- Primary completion
- 15 Jul 2026 (actual)
- Study completion
- Dec 2026 (estimated)
- First posted
- 3 Jul 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will evaluate if a direct-to-patient, de-centralized, remote approach will improve clinical research outreach and engagement for patients with SCLC, in the context of a bio-specimen collection study. The study will also assess self-reported preferences and needs of patients with SCLC, regarding choosing and accessing novel therapies in research or standard clinical care settings and supportive gaps in this area, through an initial and 3 month follow up survey.
Detailed description
This is a non-interventional, non-treatment, non-randomized, single coordinating center, study to determine the feasibility of decentralized bio-specimen collection in USA-based adult subjects with SCLC, to be conducted in conformance with Good Clinical Practices. Potential study subjects will be referred to contact staff through a dedicated study webpage form or dedicated study phone hotline at the coordinating center (ALCMI) who will handle informed consent, coordinate remote blood sample collection with study subjects, and collect medical records to confirm diagnosis and treatment history. Subjects will also be asked to complete a baseline and follow up questionnaire/survey documenting their self-report diagnosis, treatment history, factors impacting care and quality of life, and needs/preferences regarding supportive resources.
Patients who have been diagnosed with either extensive stage primary SCLC or patients diagnosed with primary NSCLC who experienced histological "transformation" with a SCLC component after initial diagnosis and subsequent treatment (transformed SCLC; tSCLC) will be invited to volunteer for this study.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| SCLC (primary de novo) | – | –Blood collection, survey (baseline and Month 3) |
| SCLC (transformed) | – | –Blood collection, survey (baseline and Month 3) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adults (USA-based) with a diagnosis of extensive stage primary SCLC or tSCLC
Key inclusion criteria (6 listed)
- Men or women greater than or equal to 18 years of age at the time of consent
- Ability to read, write and communicate in English
- Provide voluntary consent to participate in this study, documented via a signed informed Consent Form (ICF)
- Willing to provide clinical and medical information related to his/her cancer diagnoses to the study team as required
- Willing to comply with the requirements of the study
Key exclusion criteria (3 listed)
- Known existence of an uncontrolled intercurrent illness including, but not limited to, psychiatric illness or social situations that would impair compliance with study requirements
- Subjects who previously enrolled to this study
- Note: Concurrent enrollment in other clinical trials is NOT exclusionary
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Feasibility of conducting trial in SCLC population
Time frame: 12 months
Percentage of overall eligible subjects enrolled. Percentage of primary SCLC eligible subjects enrolled. Percentage of tSCLC eligible subjects enrolled. Percentage of SCLC eligible subjects enrolled compared to percentage of tSCLC eligible subjects enrolled. Percentage of primary SCLC enrolled subjects completed. Percentage of tSCLC enrolled subjects completed. Percentage of SCLC enrolled subjects completed compared to percentage of tSCLC enrolled subjects completed. Overall reasons for early termination. Reasons for early termination from trial in primary SCLC enrolled. Reasons for early termination from trial in tSCLC enrolled.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Aug 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Christine Lovly, MD PhD principal investigator
Vanderbilt-Ingram Cancer Center
52 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Small-cell Lung Cancer, run by Addario Lung Cancer Medical Institute at 52 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 4 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 52 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Feasibility of conducting trial in SCLC population (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Aug 2026.