Humanised antibodies and uses thereof
AssigneeTelix Pharmaceuticals (Innovations) Pty Ltd.
InventorsMichael Paul WHEATCROFT, David CHIN, Alesia IVASHKEVICH, Alexander Hugo STAUDACHER, Michael Paul BROWN
Life of this patent
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Abstract
The invention relates to humanised antibodies for binding to the La/SSB antigen, antigen binding fragments derived therefrom, compositions comprising the antibodies or antigen binding fragments thereof, and uses thereof in methods of treatment.
Claims71
An antigen binding protein for binding to La/SSB antigen, wherein the antigen binding protein comprises:
- i. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 3, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 6, wherein the CDRs are defined according to Kabat nomenclature;
- ii. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 1, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 5;
- iii. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 1, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 6, wherein the CDRs are defined accordingly to Kabat nomenclature;
- iv. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 2, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 4;
- v. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 2, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 5;
- vi. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 2, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 6;
- vii. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 3, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 4, wherein the CDRs are defined accordingly to Kabat nomenclature;
- or
- viii. a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable heavy chain as defined in SEQ ID NO:
- 3, and a CDR1, a CDR2 and a CDR3 of an antigen binding domain having a variable light chain as defined in SEQ ID NO:
- 5.
The immunoglobulin of claim conjugated to a radionuclide.
A method of treating a subject with a cytotoxic agent, the method comprising:
- administering a cytotoxic agent to a subject, or providing a subject who has been administered a treatment with a cytotoxic agent,
- administering an antigen binding protein as described herein to the subject, wherein the antigen binding protein comprises a detectable moiety for enabling detection thereof,
- detecting the antigen binding protein in the subject,
- determining to continue or continuing to administer the cytotoxic agent to the subject when the detection of the antigen binding protein in the subject is above a background level;
- or
- determining to discontinue or discontinuing to administer the cytotoxic agent to the subject when the detection of the antigen binding protein in the subject is the same or lower than a background level, optionally determining to administer or administering an increased dose of the cytotoxic agent or an alternative or supplemental treatment to the subject.
A method of treating a subject with a cytotoxic agent, the method comprising:
- administering a cytotoxic agent to a subject, or providing a subject who has been administered a treatment with a cytotoxic agent,
- administering an antigen binding protein as described herein to the subject, wherein the antigen binding protein comprises a detectable moiety for enabling detection thereof,
- detecting the antigen binding protein in the subject,
- determining to continue or continuing to administer the cytotoxic agent to the subject based on the output of a machine learning model or algorithm indicating the presence or increased presence of La antigen in the subject;
- determining to discontinue or discontinuing to administer the cytotoxic agent to the subject based on the output of a machine learning model or algorithm indicating an absence of La antigen in the subject, optionally determining to administer or administering an increased dose of the cytotoxic agent or an alternative or supplemental treatment to the subject.
A method of treating, preventing or minimising progression of a disease or condition, preferably of cancer, in a subject, minimising, reducing or preventing growth of a tumor in a subject, minimising, reducing or preventing metastasis in a subject, or increasing survival of a subject, the method comprising:
- providing a subject who has received a first cytotoxic therapy;
- and
- administering to the subject, a second cytotoxic therapy in the form of an antigen binding protein as described herein, wherein the antigen binding protein is conjugated to, or associated with, a cytotoxic agent,
- thereby treating, preventing or minimising progression of a disease or condition, preferably of cancer, in a subject;
- or minimising, reducing or preventing growth of a tumour in a subject, or minimising, reducing or preventing metastasis in a subject, or increasing survival of a subject.
Dependencies are inferred from the claim text.