COSELA shields helping to protect a neutrophil and red blood cell while a chemotherapy arrow targets cancer cells

To decrease the incidence of chemotherapy-induced myelosuppression in patients when administered prior to a platinum/etoposide-containing regimen or topotecan-containing regimen

For extensive-stage small cell lung cancer (ES-SCLC)

SPARE THE MARROW. SPEAR THE TUMOR.

COSELA HELPS PROTECT AGAINST myelosuppression, while chemotherapy targets cancer cells

COSELA® (trilaciclib) helps protect hematopoietic stem and progenitor cells (HSPCs), the source of blood cell lineages, including neutrophils, red blood cells, and platelets

The First and Only Proactive Multilineage Myeloprotection Therapy

Neutrophil cell Neutrophil cell

In the Pivotal Study in 1st-Line ES-SCLC, COSELA administered before an etoposide/carboplatin + atezolizumab (E/P/A) regimen resulted in1:

Primary Endpoints: 1.9% vs 49.1% (P<0.0001) and 0 days vs 4 days (P<0.0001) with and without COSELA, respectively*

Secondary Endpoints: 19% vs 28% and 13% vs 21% with and without COSELA, respectively

Secondary Endpoint: 1.9% vs 37.7% with and without COSELA (P=0.0026)

Secondary Endpoint: 2.1 vs 8.5 with and without COSELA (P=0.0195)§

* Multiplicity-adjusted P values. Adjusted relative risk (aRR) 0.038 (95% CI, 0.008, 0.195) and mean difference -3.6 (95% CI, -4.9, -2.3), respectively. Duration evaluated in Cycle 1.
aRR 0.663 (95% CI, 0.336, 1.310) and aRR 0.642 (95% CI, 0.294, 1.404). Red blood cell (RBC) transfusions measured on/after 5 weeks. Grade 3/4 anemia defined as Grade 3/4 decreased hemoglobin.
Raw one-sided P value not adjusted for multiplicity. aRR 0.053 (95% CI, 0.008, 0.356). Platelet endpoint results were not consistent across studies. See  Study 2. See  Study 3.
§ Raw one-sided P value not adjusted for multiplicity. Rate of all-cause dose reductions, events per 100 cycles. aRR 0.242 (95% CI, 0.079, 0.742).

Standard-of-care supportive interventions, including RBC and platelet transfusions, were allowed per investigator discretion throughout the entire treatment period. Primary prophylaxis with granulocyte colony-stimulating factors (G-CSFs) and use of erythropoiesis stimulating agents (ESAs) were prohibited in Cycle 1 of induction, although therapeutic G-CSF was allowed in all cycles. More patients in the E/P/A regimen arm without COSELA received G-CSF Administration (47.2% vs 29.6%, aRR 0.646 [95% CI, 0.403, 1.034]) and had ESA use (11% vs 6%, aRR 0.529 [95% CI, 0.145, 1.927]) vs with COSELA, respectively.

See Study Design >

See Multilineage Efficacy >
HEAR FROM A PEER

COSELA: A STANDARD OF CARE

INTEGRATED SAFETY ACROSS STUDIES

The most common adverse reactions (≥10%) were fatigue, hypocalcemia, hypokalemia, hypophosphatemia, aspartate aminotransferase increased, headache, and pneumonia.

See Safety Data >

THE FIRST & ONLY MYELOPROTECTION THERAPY

COSELA helps protect hematopoietic stem and progenitor cells (HSPCs), the source of multiple blood cell lineages, including neutrophils, red blood cells, and platelets. Watch the COSELA mechanism of action (MOA) video to learn about the proactive and multilineage MOA.

Additionally, find key insights from a leading medical oncologist.

Explore the MOA >