Addressing the unmet need in mCRC

Extending survival in mCRC remains an important need despite prior advances.^1,2

Colorectal cancer (CRC) is often deadly:

of patients with CRC will experience metastatic disease, whether at diagnosis or over the course of treatment¹

5-year relative survival rate for patients with distant mCRC⁴

The incidence of mCRC in patients younger than 50 has historically been low, but recently, the number of cases has increased dramatically.^2,3

Despite a majority of patients with mCRC being ≥65 years of age between 2010 and 2019, the greatest increase in mCRC was seen in younger patients.³

Between 2010 and 2019, there was a 22.1% increase in patients 18 to 49 years of age, a 14.9% increase in patients 50 to 64 years of age, and a 21.6% increase in patients greater or equal to 65 years old.

Understanding the underlying causes and the treatment options for patients of all ages remains critical in oncology.

FRUZAQLA Patient Profiles

Learn about patient types and why they may benefit from FRUZAQLA.

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Support Our Veterans

Many US veterans remain at risk of developing colorectal cancer. Learn about this risk to your patients.

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You know the importance of choosing the right therapy at the right time to maximize benefits for your patients.^4-6

As mCRC progresses, fewer and fewer patients reach the next line of treatment, with more patients facing disease progression or choosing to transition to BSC.

Real-World Data Reveals:

In real world settings, 25% to 30% of patients advance after 2 prior treatments. 10% to 15% of patients advance after 3 prior treatments.

Designed for patients with mCRC

Discover how FRUZAQLA could meet the needs of patients with previously treated metastatic colorectal cancer.

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Clinical Results With FRUZAQLA

Learn about the efficacy results from the FRESCO and FRESCO-2 studies in patients with previously treated mCRC.

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FRUZAQLA Safety Profile

Learn about safety profile from the FRESCO and FRESC) studies in patients with previously treated mCRC.

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^aCoverage relevant to your patients may vary and is subject to change without notice. Status is representative of the coverage for the majority of members covered under each plan. This information is not intended to give advice or promise coverage or payment. Contact the plan for more information about current coverage, restrictions, or requirements that may apply.

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

Hypertension occurred in 49% of 911 patients with mCRC treated with FRUZAQLA, including Grade 3-4 events in 19%, and hypertensive crisis in three patients (0.3%). Do not initiate FRUZAQLA unless blood pressure is adequately controlled. Monitor blood pressure weekly for the first month and at least monthly thereafter as clinically indicated. Initiate or adjust anti-hypertensive therapy as appropriate. Withhold, reduce dose, or permanently discontinue FRUZAQLA based on severity of hypertension.

Hemorrhagic Events including serious, fatal events can occur with FRUZAQLA. In 911 patients with mCRC treated with FRUZAQLA, 6% of patients experienced gastrointestinal hemorrhage, including 1% with a Grade ≥3 event and 2 patients with fatal hemorrhages. Permanently discontinue FRUZAQLA in patients with severe or life-threatening hemorrhage. Monitor the International Normalized Ratio (INR) levels in patients receiving anticoagulants.

Infections. FRUZAQLA can increase the risk of infections, including fatal infections. In 911 patients with mCRC treated with FRUZAQLA, the most common infections were urinary tract infections (6.8%), upper respiratory tract infections (3.2%) and pneumonia (2.5%); fatal infections included pneumonia (0.4%), sepsis (0.2%), bacterial infection (0.1%), lower respiratory tract infection (0.1%), and septic shock (0.1%). Withhold FRUZAQLA for Grade 3 or 4 infections, or worsening infection of any grade. Resume FRUZAQLA at the same dose when the infection has resolved.

Gastrointestinal Perforation occurred in patients treated with FRUZAQLA. In 911 patients with mCRC treated with FRUZAQLA, 1.3% experienced a Grade ≥3 gastrointestinal perforation, including one fatal event. Permanently discontinue FRUZAQLA in patients who develop gastrointestinal perforation or fistula.

Hepatotoxicity. FRUZAQLA can cause liver injury. In 911 patients with mCRC treated with FRUZAQLA, 48% experienced increased ALT or AST, including Grade ≥3 events in 5%, and fatal events in 0.2% of patients. Monitor liver function tests (ALT, AST, and bilirubin) before initiation and periodically throughout treatment with FRUZAQLA. Temporarily hold and then reduce or permanently discontinue FRUZAQLA depending on the severity and persistence of hepatotoxicity as manifested by elevated liver function tests.

Proteinuria. FRUZAQLA can cause proteinuria. In 911 patients with mCRC treated with FRUZAQLA, 36% experienced proteinuria and 2.5% of patients experienced Grade ≥3 events. Monitor for proteinuria before initiation and periodically throughout treatment with FRUZAQLA. For proteinuria ≥2g/24 hours, withhold FRUZAQLA until improvement to ≤Grade 1 proteinuria and resume FRUZAQLA at a reduced dose. Discontinue FRUZAQLA in patients who develop nephrotic syndrome.

Palmar-Plantar Erythrodysesthesia (PPE) occurred in 35% of 911 patients treated with FRUZAQLA, including 8% with Grade 3 events. Based on severity of PPE, withhold FRUZAQLA and then resume at the same or reduced dose.

Posterior Reversible Encephalopathy Syndrome (PRES), a syndrome of subcortical vasogenic edema diagnosed by characteristic finding on MRI, occurred in one of 911 patients treated with FRUZAQLA. Perform an evaluation for PRES in any patient presenting with seizures, headache, visual disturbances, confusion, or altered mental function. Discontinue FRUZAQLA in patients who develop PRES.

Impaired Wound Healing. In 911 patients with mCRC treated with FRUZAQLA, 1 patient experienced a Grade 2 event of wound dehiscence. Do not administer FRUZAQLA for at least 2 weeks prior to major surgery. Do not administer FRUZAQLA for at least 2 weeks after major surgery and until adequate wound healing. The safety of resumption of FRUZAQLA after resolution of wound healing complications has not been established.

Arterial Thromboembolic Events. In 911 patients with mCRC treated with FRUZAQLA, 0.8% of patients experienced an arterial thromboembolic event. Initiation of FRUZAQLA in patients with a recent history of thromboembolic events should be carefully considered. In patients who develop arterial thromboembolism, discontinue FRUZAQLA.

Allergic Reactions to FD&C Yellow No. 5 (Tartrazine) and No. 6 (Sunset Yellow FCF). FRUZAQLA 1 mg capsules contain FD&C Yellow No. 5 (tartrazine), which may cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. FRUZAQLA 1 mg contains FD&C Yellow No. 6 (sunset yellow FCF), which may cause allergic reactions.

Embryo-Fetal Toxicity. Based on findings in animal studies and its mechanism of action, FRUZAQLA can cause fetal harm when administered to pregnant women. Advise pregnant women of the potential risk to a fetus.

ADVERSE REACTIONS

The most common adverse reactions (incidence ≥20%) following treatment with FRUZAQLA included hypertension, palmar-plantar erythrodysesthesia (hand-foot skin reactions), proteinuria, dysphonia, abdominal pain, diarrhea, and asthenia.

DRUG INTERACTIONS

Avoid concomitant administration of FRUZAQLA with strong or moderate CYP3A inducers.

USE IN SPECIFIC POPULATIONS

Lactation: Advise women not to breastfeed during treatment with FRUZAQLA and for 2 weeks after the last dose.

Females and Males of Reproductive Potential

Pregnancy Testing: Verify pregnancy status of females of reproductive potential prior to initiating FRUZAQLA.
Contraception: Females of childbearing potential and males with female partners of childbearing potential should use effective contraception during treatment and for 2 weeks after the last dose of FRUZAQLA.
Infertility: Advise females of reproductive potential that FRUZAQLA may cause post-implantation loss.

To report SUSPECTED ADVERSE REACTIONS, contact Takeda Pharmaceuticals at 1-844-662-8532 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Please see FRUZAQLA (fruquintinib) full Prescribing Information.

Addressing the unmet need in mCRC

Extending survival in mCRC remains an important need despite prior advances.^1,2

Colorectal cancer (CRC) is often deadly:

The incidence of mCRC in patients younger than 50 has historically been low, but recently, the number of cases has increased dramatically.^2,3

FRUZAQLA Patient Profiles

Support Our Veterans

You know the importance of choosing the right therapy at the right time to maximize benefits for your patients.^4-6

Designed for patients with mCRC

Clinical Results With FRUZAQLA

FRUZAQLA Safety Profile

IMPORTANT SAFETY INFORMATION AND INDICATION

WARNINGS AND PRECAUTIONS

ADVERSE REACTIONS

DRUG INTERACTIONS

USE IN SPECIFIC POPULATIONS

INDICATION

Extending survival in mCRC remains an important need despite prior advances.1,2

Colorectal cancer (CRC) is often deadly:​

The incidence of mCRC in patients younger than 50 has historically been low, but recently, the number of cases has increased dramatically.2,3

FRUZAQLA Patient Profiles

Support Our Veterans

You know the importance of choosing the right therapy at the right time to maximize benefits for your patients.4-6

Designed for patients with mCRC

Clinical Results With FRUZAQLA

FRUZAQLA Safety Profile

IMPORTANT SAFETY INFORMATION AND INDICATION

Extending survival in mCRC remains an important need despite prior advances.^1,2

Colorectal cancer (CRC) is often deadly:

The incidence of mCRC in patients younger than 50 has historically been low, but recently, the number of cases has increased dramatically.^2,3

You know the importance of choosing the right therapy at the right time to maximize benefits for your patients.^4-6