Combination Treatment of Belantamab Mafodotin and Venetoclax in Treatment of Relapsed and Refractory T(11;14) Multiple Myeloma

Relapsed and refractory t(11;14) Multiple Myeloma (RRMM)

Inclusion criteria:

1. Subjects must be ≥ 18 years of age.

2. Subjects must have an Eastern Cooperative Oncology Group (ECOG) performance statusof ≤ 2

3. Subjects must voluntarily sign and date an in-formed consent form

4. Subjects must have had documented multiple myeloma requiring treatment as defined bythe criteria below: Monoclonal plasma cells in the bone marrow > 10% and/or presence of a biopsy provenplasmacytoma at some point in their disease history requiring treatment accordingdiag-nostic criteria (IMWG updated criteria 2014, Rajkumar et al. 2014) withmeasurable dis-ease at screening (serum M-protein > 500 mg/dL or urine M protein 200mg/24h, in case of oligosecretory MM serum free light chain > 10mg/dL and abnormalkap-pa/lambda free light chain ratio)

5. Cytogenetics/FISH confirming t(11;14)

6. Prior treatment requirements: Prior treatment requirements: a. Subjects must have received at least 1 prior treatment line (induction,high-dose, consolidation and maintenance is considered as one treatment line). Allpatients have to have received at least one proteasome inhibitor and at least oneimmunomodulatory agent and at least one anti-CD38 monoclonal antibody. b. Subjects must have documented evidence of progressive disease on or after thelast treatment line. c. Subjects with a history of autologous SCT are eligible for study participationprovided the following eligibility criteria are met: i. ASCT was >100 days prior toinitiating study treatment, and ii. No active bacterial, viral, or fungalin-fection(s) present.

7. Subjects must have adequate organ function, defined as follows: a. Hemoglobin ≥8.0 g/dL (without transfusion of red blood cells for the past 14days) b. Absolute neutrophil count ≥ 1.5 x109/L (with-out growth factor support forthe past 14 days) c. Platelet count more or equal 75 x109/L (with-out growth factoror platelet stimulating agents for the past 14 days) d. Adequate hepatic functionper local laborato-ry reference range as follows: i. Aspartate aminotransferase (AST) ≤ 2,5 x upper limit of normal (ULN); ii. Alanine aminotransferase (ALT) ≤ 2.5x ULN iii. Total bilirubin ≤ 1.5 x ULN, except in subjects with congenitalbilirubinemia, such as Gilbert syndrome (direct bili-rubin ≤ 1.5 x ULN). Isolatedbilirubin ≥1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%. e. Subjects must have adequate renal function as demonstrated by eGFR ≥30 mL/min/ 1.73 m2 as calculated by Modified Diet in Renal Disease (MDRD) formula f. Spot urine (albumin/creatinine ratios (spot urine) <500 mg/g (56 mg/mmol) OR Urine DipstickNegative/trace (if 1+ only eligible if confirmed <500 mg/g (56 mg/mmol) byalbumin/creatinine ratio (spot urine from first void) g. Corrected serum calcium ≤ 14 mg/dL (≤3,5 mmol/L); or free ionized calcium ˂ 6,5 mg/dL (˂1,6 mmol/L)

8. A female participant is eligible to participate if she is not pregnant orbreastfeeding, and at least one of the following conditions applies:

9. Is not a woman of childbearing potential (WOCBP) OR

10. Is a WOCBP and using a contraceptive method that is highly effective

11. Male participants are eligible to participate if they agree to the refrain fromdonating sperm and either bei abstinent from heterosexual intercourse or agree touse a highly effective contraceptive method during the intervention period and for 6months after the last dose of study treatment to allow for clearance of any alteredsperm

12. All subjects must agree to refrain from donating blood while on study drug and for 28 days after discontinuation from this study treatment.

13. All subjects must agree not to share study medication.

14. All prior treatment-related toxicities (defined by National Cancer Institute- CommonToxicity Criteria for Adverse Events (NCI-CTCAE), version 5.0) must be ≤ Grade 1 atthe time of en-rolment except for alopecia.

Exclusion Criteria:

1. Subject has received prior Venetoclax and/or anti BCMA treatment.

2. Participant has used an investigational drug or approved systemic anti-myelomatherapy with-in 14 days or five half-lives, whichever is short-er, preceding thefirst dose of study drug. The only exception is emergency use of a short course ofcorticosteroids (equivalent of Dexa-methasone 40 mg/day for a maximum of 4 days) upto 7 days before treatment.

3. Participant has had plasmapheresis or radia-tion therapy within 7 days prior tofirst dose of study treatment

4. Participant has current corneal epithelial dis-ease except mild changes in cornealepitheli-um

5. Participant has current unstable liver or biliary disease

6. Participant has a presence of active renal con-dition (infection, requirement fordialysis or any other condition that could affect participant's safety).

7. Participant has had major surgery ≤ 4 weeks prior to initiating study treatment.Kyphoplasty is not considered a major surgery.

8. Participant must not use contact lenses while participating in this study. Bandagecontacts may be prescribed by an eye care professional if needed.

9. Participant has any evidence of active mucosal or internal bleeding or othergastrointestinal disease that may significantly alter the absorp-tion of oral drugs.

10. Participant has evidence of cardiovascular risk as defined in the protocol

11. Participant has known immediate or delayed hypersensitivity reaction oridiosyncratic reac-tions to IMPs or drugs chemically related to IMPs, or any of thecomponents of the study treatment

12. Participant has an invasive malignancy other than disease under study within 5 yearsbefore trial inclusion, except

• Adequately treated in situ carcinoma of the cervix uteri or the breast;

• Basal cell carcinoma of the skin or localized squamous cell carcinoma of theskin;

• Prostate cancer Gleason grade 6 or lower AND with stable Prostate SpecificAntigen (PSA) levels off treatment;

• Previous malignancy with no current evi-dence of disease, and which wasconfined and surgically resected (or treated with other mo-dalities) withcurative intent and unlikely to im-pact survival during the duration of thestudy.

13. Participant is pregnant or lactating

14. Participants who have had prior allogeneic stem cell transplant.

15. Participants with symptomatic amyloidosis, ac-tive POEMS syndrome (polyneuropathy,or-ganomegaly, endocrinopathy, monoclonal plasmaproliferative disorder, skinchanges) or active plasma cell leukaemia at the time of screening.

16. Participants with any serious and/or unstable pre-existing medical, psychiatricdisorder or other conditions (including lab abnormalities) that could interfere withparticipant's safety, ob-taining informed consent or compliance to the studyprocedures.

17. Subject is known to be seropositive for human immunodeficiency virus (HIV) orhepatitis B (defined by a positive test for hepatitis B sur-face antigen (HBsAg) orantibodies to hepatitis B surface and core antigen (anti HBs and anti HBcrespectively), or hepatitis C (anti-HCV an-tibody positive or HCV RNA quantitationposi-tive).

18. Current immune or inflammatory conditions re-quiring immunosuppressive treatment (e.g. systemic lupus erythematosus, rheumatoid ar-thritis).

19. Subject must not have received any live vac-cines within 8 weeks prior to first doseof study treatment.

20. Subject must not use or anticipate the use of prohibited medications or foods duringstudy participation.

21. Subject does not have a history of or show any signs of known meningeal/centralnervous sys-tem involvement by myeloma.

22. Evidence of other clinically significant uncon-trolled condition(s) that is likelyto interfere with the study proce-dures or results, or that in the opinion of theinvestigator, would constitute a hazard for the participation in this study.

23. Subject is known or suspected of not being able to comply with the study protocol.Subject has any condition for which, in the opinion of the investigator,participation would not be in the best interest of the subject (e.g., compromise thewell-being) or that could prevent, limit or confound the pro-tocol-specifiedassessments.

24. Treatment with any of the following within 7 days prior to the first dose of studydrug:

25. moderate or strong cytochrome P450 3A (CYP3A) inhibitors

26. moderate or strong CYP3A inducers

27. Administration or consumption of any of the fol-lowing within 3 days prior to thefirst dose of study drug:

28. grapefruit or grapefruit products

29. Seville oranges (including marmalade con-taining Seville oranges)

30. star fruit

31. Participation in any other clinical trial (with the exclusion of observationalstudies)