CML Referral Facilitation
Chronic Myeloid Leukemia
Referral Facilitation
Chronic Myeloid Leukemia
Referral Facilitation
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Please complete this form if you are interested in connecting with a staff member at Terns Pharmaceuticals in order to facilitate referral into the CARDINAL clinical trial of eligible patients with previously treated CP-CML.
Once you complete the form a staff member will contact you as soon as possible in order to facilitate the referral of patients to an active clinical trial site near you.
Additional information about this clinical trial can be found here.
Key Inclusion Criteria:
Male or female participants ≥ 18 years of age at the time of signing the informed consent
Have an ECOG performance status score of 0 to 2
Have an established cytopathologically confirmed diagnosis of BCR-ABL1 positive CML in Chronic Phase with or without T315l mutation
Have received treatment with active site targeting TKIs and have treatment failure, suboptimal response, or treatment intolerance
Participants who are intolerant of asciminib, and do not have resistant/relapsing disease
Adequate organ function, as assessed by local laboratory
Key Exclusion Criteria:CML in accelerated or blast phase
Systemic antineoplastic therapy (including prior TKIs, interferon-alfa, therapeutic antibodies, chemotherapy) or other experimental therapy 7 days before the first dose of TERN-701
Have completed previous anticancer therapy without resolution of all associated clinically significant toxicity (to ≤ Grade 2 or baseline)
Please complete this form if you are interested in connecting with a staff member at Terns Pharmaceuticals in order to facilitate referral into the CARDINAL clinical trial of eligible patients with previously treated CP-CML.
Once you complete the form a staff member will contact you as soon as possible in order to facilitate the referral of patients to an active clinical trial site near you.
Additional information about this clinical trial can be found here.
Key Inclusion Criteria:
Male or female participants ≥ 18 years of age at the time of signing the informed consent
Have an ECOG performance status score of 0 to 2
Have an established cytopathologically confirmed diagnosis of BCR-ABL1 positive CML in Chronic Phase with or without T315l mutation
Have received treatment with active site targeting TKIs and have treatment failure, suboptimal response, or treatment intolerance
Participants who are intolerant of asciminib, and do not have resistant/relapsing disease
Adequate organ function, as assessed by local laboratory
Key Exclusion Criteria:
CML in accelerated or blast phase
Systemic antineoplastic therapy (including prior TKIs, interferon-alfa, therapeutic antibodies, chemotherapy) or other experimental therapy 7 days before the first dose of TERN-701
Have completed previous anticancer therapy without resolution of all associated clinically significant toxicity (to ≤ Grade 2 or baseline)
Please complete this form if you are interested in connecting with a staff member at Terns Pharmaceuticals in order to facilitate referral into the CARDINAL clinical trial of eligible patients with previously treated CP-CML.
Once you complete the form a staff member will contact you as soon as possible in order to facilitate the referral of patients to an active clinical trial site near you.
Additional information about this clinical trial can be found here.
Key Inclusion Criteria:
Male or female participants ≥ 18 years of age at the time of signing the informed consent
Have an ECOG performance status score of 0 to 2
Have an established cytopathologically confirmed diagnosis of BCR-ABL1 positive CML in Chronic Phase with or without T315l mutation
Have received treatment with active site targeting TKIs and have treatment failure, suboptimal response, or treatment intolerance
Participants who are intolerant of asciminib, and do not have resistant/relapsing disease
Adequate organ function, as assessed by local laboratory
Key Exclusion Criteria:CML in accelerated or blast phase
Systemic antineoplastic therapy (including prior TKIs, interferon-alfa, therapeutic antibodies, chemotherapy) or other experimental therapy 7 days before the first dose of TERN-701
Have completed previous anticancer therapy without resolution of all associated clinically significant toxicity (to ≤ Grade 2 or baseline)
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Ready to Supercharge ⚡ Treatment Development & Launch?
Fill out the contact form, and our team will reach out to schedule a meeting.
Project: Tolv Studio
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Ready to Supercharge ⚡ Treatment Development & Launch?
Fill out the contact form, and our team will reach out to schedule a meeting.
Project: Tolv Studio
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Ready to Supercharge ⚡ Treatment Development & Launch?
Fill out the contact form, and our team will reach out to schedule a meeting.
Project: Tolv Studio


Ready to Supercharge ⚡ Treatment Development & Launch?
Fill out the contact form, and our team will reach out to schedule a meeting.
Project: Tolv Studio