CML Referral Facilitation

Chronic Myeloid Leukemia
Referral Facilitation

Chronic Myeloid Leukemia
Referral Facilitation

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)

CML Patient Referral Form

CML Patient Referral Form

Ready to Supercharge ⚡ Treatment Development & Launch?

Fill out the contact form, and our team will reach out to schedule a meeting.

© 2025 Adnexi All rights reserved.

Project: Tolv Studio

Ready to Supercharge ⚡ Treatment Development & Launch?

Fill out the contact form, and our team will reach out to schedule a meeting.

© 2025 Adnexi All rights reserved.

Project: Tolv Studio

Ready to Supercharge ⚡ Treatment Development & Launch?

Fill out the contact form, and our team will reach out to schedule a meeting.

© 2025 Adnexi All rights reserved.

Project: Tolv Studio

Ready to Supercharge ⚡ Treatment Development & Launch?

Fill out the contact form, and our team will reach out to schedule a meeting.

© 2025 Adnexi All rights reserved.

Project: Tolv Studio