ClinicalTrials.gg
RecruitingNCT07473128Updated Oct 2, 2026

Effect of Trilaciclib in the Prevention of Myelosupression in Subjects With Limited-stage Small Cell Lung Cancer

A Phase 3 interventional study of Trilaciclib and Saline (0.9% NaCl) in Limited Stage Small Cell Lung Cancer, sponsored by Pharmacosmos A/S. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-02.

Sponsored by Pharmacosmos A/S · Phase 3, Interventional, and Supportive care

Updated Oct 2, 2026Start date movedPrimary completion moved+1 moreGo to Updates ↓
Phase
Phase 3
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 629 studies in Small Cell Lung Carcinoma with a site in United States — 112 open to participants now, 182 under way, 27 of them phase 3. Small Cell Lung Carcinoma · United States.

Planned enrollment
166th of 550
120 · median 55
Started
2026
with 36 others
Phase 3
51 of 629
11 open now
Primary completion
2027-10
later than 79 of 181 live
Registered
609th of 629
by date

Among the 629 studies in Small Cell Lung Carcinoma with a site in United States, this one is the 166th largest by planned enrollment of the 550 interventional ones that give a count, is one of 37 that started in 2026, is one of 51 in phase 3, reaches primary completion later than 79 of the 181 other live ones, and was the 609th registered.

Small Cell Lung Carcinoma

1,301 studies on the registry are indexed under Small Cell Lung Carcinoma; 367 are open to participants now.

This study's planned enrollment of 120 is above the median of 56 across 1,077 interventional studies indexed under Small Cell Lung Carcinoma.

Browse Small Cell Lung Carcinoma studies →

Open to participants now

112 of the 629 studies in Small Cell Lung Carcinoma with a site in United States are open now.

All 112 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 264 Small Cell Lung Carcinoma studies recruiting now, 173 (66%) set no upper age limit and 67 (25%) stop at 75 or younger; 3 take children under 18; 8 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →
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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 629 studies in Small Cell Lung Carcinoma with a site in United States, or all of them as a file.
02

Study summary

The goal of this clinical trial is to compare the efficacy and safety of trilaciclib versus placebo in subjects with limited stage small cell lung cancer. The main question it aims to answer is:

Does trilaciclib have a myeloprotective effect in subject with limited stage small cell lung cancer?

Participants will be randomised to receive either trilaciclib or placebo.

03

Conditions studied

  • Limited Stage Small Cell Lung Cancer
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Confirmed diagnosis of Limited-Stage Small Cell Lung Cancer
  • Complete recovery from prior anti-tumor surgical procedures
  • Measurable and evaluable disease through tumor assessment
  • Willingness to participate and sign form

Exclusion criteria

Exclusion Criteria:

  • Extensive Stage Small Cell Lung Cancer
  • Active cardiovascular disease
  • Known to trilaciclib, etoposide, carboplatin, cisplatin or any component in their formulations
  • Pregnant or nursing women
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 3
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Trilaciclib

    Receives trilaciclib

    Drug: Trilaciclib

  • Placebo comparator
    Placebo

    Receives placebo

    Drug: Saline (0.9% NaCl)

Interventions

  • Intravenous infusion

  • DrugSaline (0.9% NaCl)

    Intravenous infusion

    Also known as: dextrose

06

What researchers measure

Primary outcomes

  1. To Compare trilaciclib to placebo on prevention of myelosuppression

    Duration and occurrence of severe neutropenia

    Time frame: From enrollment and 4 months after

Secondary outcomes

  1. Number of all-cause chemotherapy dose reductions

    Time frame: From enrollment and 4 months after

  2. Occurrence of granulocyte colony-stimulating factor (G-CSF) administration

    Time frame: From enrollment and 4 months after

  3. Number of hospitalizations due to myelosuppression or sepsis

    Time frame: From enrollment and 4 months after

  4. Number of febrile neutropenia

    Time frame: From enrollment and 4 months after

  5. Occurrence of red blood cell (RBC) transfusions

    Time frame: From enrollment and 4 months after

07

Study locations

1 of 1 sites recruiting
  • Pharmacosmos Investigational Site
    Oakland, California 48073, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Oct 2027, 13 months later.

Of 56 industry-sponsored phase 3 interventional studies under Small Cell Lung Carcinoma, half reached primary completion within 36 months of starting (the median), counting those still running; a quarter within 30 and three quarters within 44. This study's planned 13 months is below that.

Counting every sponsor, half of 69 studies reached it within 44 months; a quarter within 31 and three quarters within 48.

Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 2, 2026: start Jun 2026 → Sep 2026, primary completion Jun 2027 → Oct 2027 and completion Jun 2027 → Oct 2027.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Mar 5, 2026
First posted
Mar 16, 2026
StartEst.
Sep 2026was Jun 2026
Primary completionEst.
Oct 31, 2027was Jun 2027
CompletionEst.
Oct 31, 2027was Jun 2027
Last update
Oct 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Start date
Jun 30, 2026→Sep 2026
Oct 2, 2026
Primary completion
Jun 2027→Oct 31, 2027
Oct 2, 2026
Study completion
Jun 2027→Oct 31, 2027
Oct 2, 2026
Show all 1 update
  1. Oct 2, 2026
    Start date Jun 30, 2026→Sep 2026
    Primary completion Jun 2027→Oct 31, 2027
    Study completion Jun 2027→Oct 31, 2027
    + 2 other changes: verification date and contact details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07473128
Lead sponsor
Pharmacosmos A/S
Responsible party
Sponsor
First posted
Mar 16, 2026
Start date
Sep 2026 (estimated)
Primary completion
Oct 31, 2027 (estimated)
Completion
Oct 31, 2027 (estimated)
Last update
Oct 2, 2026

Study contacts

Pharmacosmos A/S Clinical and non-clinical research
Contact
info@pharmacosmos.com
+4559485959

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Trilaciclib

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