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3178 Updated Results from the Phase 3 Manifest-2 Study of Pelabresib in Combination with Ruxolitinib for Janus Kinase Inhibitor–Naïve Patients with Myelofibrosis

Program: Oral and Poster Abstracts
Session: 634. Myeloproliferative Syndromes: Clinical and Epidemiological: Poster II
Hematology Disease Topics & Pathways:
Research, Combination therapy, Drug development, Clinical Research, Diseases, Treatment Considerations, Myeloid Malignancies, Study Population, Human
Sunday, December 8, 2024, 6:00 PM-8:00 PM

John O. Mascarenhas, MD1, Sebastian Grosicki, MD, PhD2*, Dominik Chraniuk, MD3*, Elisabetta Abruzzese, MD4, Prithviraj Bose, MD5, Aaron T. Gerds, MD, MS6, Alessandro M. Vannucchi, MD, PhD7, Francesca Palandri, MD, PhD8*, Sung-Eun Lee, MD, PhD9*, Vikas Gupta, MD, FRCP, FRCPath10, Alessandro Lucchesi, MD, PhD11*, Stephen Oh, MD, PhD12, Andrew T. Kuykendall, MD13, Andrea Patriarca, MD14*, Alberto Alvarez-Larran15*, Ruben Mesa, MD16*, Jean-Jacques Kiladjian, MD, PhD17, Moshe Talpaz, MD18, Morgan Harris, PharmD19*, Sarah-Katharina Kays, PhD20*, Qing Li, PhD21*, Barbara Brown, PhD19*, Anna-Maria Jegg, PhD20*, Claire Harrison22 and Raajit Rampal, MD, PhD23

1Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY
2Medical University of Silesia, Katowice, Poland
3Hematology Ward, Wojewódzki Szpital Zespolony im. L. Rydygiera, Torun, Poland
4Department of Hematology, S. Eugenio Hospital, Tor Vergata University, ASL Roma 2, Roma, I, Italy
5Leukemia Department, University of Texas MD Anderson Cancer Center, Houston, TX
6Cleveland Clinic Taussig Cancer Institute, Cleveland, OH
7Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy
8IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico S. Orsola-Malpighi, Istituto di Ematologia "Seràgnoli", Bologna, Italy
9Department of Hematology,, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea, Republic of (South)
10The Princess Margaret Cancer Centre, Toronto, ON, Canada
11Hematology Unit, IRCCS Istituto Romagnolo per lo Studio e la Cura dei Tumori (IRST) “Dino Amadori”, Meldola (FC), Italy
12Washington University School of Medicine in St. Louis, St. Louis, MO
13Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL
14Hematology Unit, AOU Maggiore della Carità and University of Eastern Piedmont, Novara, Italy
15Hematology Department, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain
16Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University School of Medicine, Winston-Salem, NC
17Clinical Investigation Center, Hôpital Saint-Louis, Université de Paris, Paris, France
18University of Michigan Comprehensive Cancer Center, Ann Arbor, MI
19Constellation Pharmaceuticals, a MorphoSys Company, Boston, MA
20MorphoSys AG, Planegg, Germany
21MorphoSys US Inc, Boston, MA
22Department of Haematology, Guy’s and St Thomas’ NHS Foundation Trust, London, United Kingdom
23Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, NY

Background

Myelofibrosis (MF) is characterized by splenomegaly, MF-associated symptoms, cytopenias (eg, anemia), and impairment of the bone marrow (BM) microenvironment (including fibrosis). Pelabresib (CPI-0610; PELA) is an investigational, oral, small molecule drug that inhibits BET proteins and subsequent BET-mediated gene expression involved in MF pathogenesis. The Phase 3 MANIFEST-2 study (NCT04603495) met its primary endpoint, showing a statistically significant higher proportion of patients (pts) with ≥35% reduction in spleen volume (SVR35) from baseline (BL) at Week (Wk) 24 with PELA+ruxolitinib (RUX) vs placebo (PBO)+RUX (p<0.001) in Janus kinase inhibitor–naïve pts with MF. PELA+RUX also showed a trend toward improved total symptom score (TSS) from BL at Wk 24, as well as improvements in multiple measures of anemia (eg, hemoglobin [Hb] response) and in the BM microenvironment, vs PBO+RUX (Rampal R, et al. Presented at ASH 2023 [Oral 628]).

Aim

To present follow-up efficacy and safety outcomes at Wk 48 from the Phase 3 MANIFEST-2 study.

Methods
Eligible pts had a DIPSS ≥intermediate-1 risk, platelet count ≥100 × 109/L, spleen volume ≥450 cm3, ≥2 symptoms with an average score ≥3 or TSS ≥10 by MF Symptom Assessment Form v4.0, peripheral blast count <5%, and ECOG PS ≤2. Pts were randomized 1:1. PELA or PBO was administered once daily for 14 consecutive days of 21-day cycles in combination with RUX, which was administered twice daily for 21-day cycles. Primary endpoint was SVR35 at Wk 24. Key secondary endpoints were absolute change in TSS and ≥50% reduction in TSS from BL (TSS50) at Wk 24. Other prespecified endpoints included SVR35 at Wk 48, absolute change in TSS and TSS50 at Wk 48, Hb response (≥1.5 g/dL mean increase from BL without transfusions in the prior 12 wks), BM fibrosis (BMF), and safety. Mutation profiles were assessed by next-generation sequencing. Informed consent was obtained from all pts.

Results

As of March 29, 2024, all pts assessed had been followed for ≥48 wks; 58.9% (126/214) and 62.0% (134/216) of pts continued on double-blind treatment in the PELA+RUX and PBO+RUX arms, respectively. Preliminary data are presented here; analyses are ongoing and data points are subject to change. At Wk 48, 56.5% (121/214) vs 37.5% (81/216) of pts had SVR35 responses in the PELA+RUX vs PBO+RUX arms, showing sustained benefit beyond Wk 24. SVR35 responders at any time were 82.2% (176/214) vs 58.3% (126/216) in the PELA+RUX vs PBO+RUX arm; loss of SVR35 response was observed in 13.1% (23/176) vs 19.8% (25/126) of pts in the PELA+RUX vs PBO+RUX arm. At Wk 48, least squares mean (standard error) absolute change in TSS was −16.24 (1.133) vs −14.11 (1.085) in the PELA+RUX vs PBO+RUX arms, with a greater difference in absolute TSS observed between treatment arms at Wk 24 and Wk 48 for pts with higher symptom burden at BL. TSS50 response at Wk 48 was 45.3% (97/214) vs 39.4% (85/216) with PELA+RUX vs PBO+RUX. Dual SVR35 and TSS50 response was observed in 36.0% (77/214) vs 19.0% (41/216) of pts in the PELA+RUX vs PBO+RUX arms at Wk 48. Hb response was observed in 12.6% (27/214; 95% confidence interval [CI], 8.17–17.07) vs 6.9% (15/216; 95% CI, 3.55–10.33) of pts in the PELA+RUX vs PBO+RUX arms, with differences between arms in mean Hb levels maintained at Wk 48; in pts with anemia (Hb BL <10 g/dL), Hb response was observed in 17.9% (12/67; 95% CI, 8.73–27.09) vs 14.1% (10/71; 95% CI, 5.99–22.18) of pts. The trend of higher rate of BMF improvement of ≥1 grade in the PELA+RUX arm vs the PBO+RUX arm continued to be observed at Wk 48. Of 426 pts evaluated for safety, ≥1 treatment-emergent adverse event (TEAE) was reported in 97.6% vs 96.7% of pts in the PELA+RUX vs PBO+RUX arms; Grade ≥3 events were reported in 56.6% vs 62.1% of pts. Rates of the most common TEAEs (≥10%) at Wk 48 in the PELA+RUX vs PBO+RUX arms were similar to rates at Wk 24. Updated efficacy and safety results, including data on BMF, mutational profile, and leukemic transformation, will be presented.

Conclusion

At Wk 48, PELA+RUX continued to show improvements in spleen volume, TSS, multiple measures of anemia, and the BM microenvironment vs PBO+RUX, impacting the four hallmarks of MF. These data suggest that PELA+RUX could lead to more profound and sustained responses in pts with MF vs PBO+RUX.

Disclosures: Mascarenhas: NS Pharma: Research Funding; Ajax: Research Funding; MorphoSys: Consultancy; Keros: Consultancy; Blueprint Medicines: Consultancy; Kartos: Consultancy, Research Funding; Disc: Consultancy; Icahn School of Medicine at Mount Sinai: Current Employment; Celgene: Consultancy, Other: Travel Support, Speakers Bureau; Novartis: Consultancy, Other: Travel Support , Research Funding, Speakers Bureau; AbbVie: Consultancy, Research Funding; Pfizer: Research Funding; Merck: Consultancy; CTI BioPharma/SOBI: Consultancy, Research Funding; Geron: Consultancy, Research Funding; Sumitomo: Consultancy; Bristol Myers Squibb: Research Funding; Karyopharm: Consultancy; PharmaEssentia: Consultancy, Research Funding; GSK: Consultancy; Roche: Consultancy; Astellas: Research Funding; Ariad: Speakers Bureau; Incyte Corporation: Consultancy, Speakers Bureau. Chraniuk: Janssen: Consultancy. Abruzzese: Ascentage: Consultancy; Novartis: Consultancy; Pfizer: Consultancy; BMS: Consultancy; MorphoSys: Consultancy; Incyte: Consultancy. Bose: Cogent: Honoraria, Research Funding; Karyopharm: Honoraria; Novartis: Honoraria; Blueprint: Honoraria, Research Funding; AbbVie: Honoraria; Disc Medicine: Research Funding; GSK: Honoraria; Ionis Pharmaceuticals: Research Funding; BMS: Honoraria, Research Funding; Telios: Research Funding; CTI Biopharma Corp: Honoraria, Research Funding; PharmaEssentia: Honoraria; MorphSys: Honoraria, Research Funding; Incyte: Honoraria, Research Funding; Astellas: Research Funding; Kartos: Honoraria, Research Funding; Pfizer: Research Funding; NS Pharma: Research Funding; Promedior: Research Funding. Gerds: Agios: Consultancy; Disc Medicine: Consultancy; PharmaEssentia: Consultancy; Rain Oncology: Consultancy; GSK: Consultancy; AbbVie: Consultancy; BMS: Consultancy. Vannucchi: AOP: Consultancy, Speakers Bureau; Incyte: Consultancy, Speakers Bureau; BMS: Consultancy, Speakers Bureau; Novartis: Consultancy, Speakers Bureau; GSK: Consultancy, Speakers Bureau; Blueprint: Consultancy, Speakers Bureau. Palandri: AOP: Consultancy, Honoraria; BMS/Celgene: Consultancy, Honoraria; Sierra Oncology: Consultancy, Honoraria; Constellation-Morphosys: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Sobi: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; CTI: Consultancy, Honoraria; Incyte: Consultancy, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Telios: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Abbvie: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Novartis: Consultancy, Honoraria. Gupta: CTI Biopharma: Consultancy, Other: Participation on a data safety or advisory board; Sierra Oncology: Consultancy, Other: Participation on a data safety or advisory board; Sumitomo Pharm: Consultancy; Constellation: Consultancy; Pfizer: Consultancy, Other: Participation on a data safety or advisory board; Daiichi Sankyo: Consultancy, Other: Participation on a data safety or advisory board; AbbVie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; GSK: Consultancy, Honoraria, Other: support for attending meetings and/or travel; BMS/Celgene: Consultancy, Other: Participation on a data safety or advisory board; Incyte: Consultancy, Other: Participation on a data safety or advisory board; Novartis: Consultancy; Roche: Membership on an entity's Board of Directors or advisory committees. Lucchesi: AOP: Consultancy; Sanofi: Consultancy, Speakers Bureau; BMS: Speakers Bureau; Novartis: Consultancy, Speakers Bureau; Grifols: Consultancy, Speakers Bureau; Amgen: Consultancy, Speakers Bureau; MorphoSys: Consultancy; Incyte: Speakers Bureau; Pfizer: Speakers Bureau; SOBI: Consultancy, Speakers Bureau; Protagonist: Consultancy. Oh: Geron: Consultancy; AbbVie: Consultancy; Sierra Oncology: Consultancy; Incyte: Consultancy; Constellation: Consultancy; PharmaEssentia: Consultancy; Blueprint Medicines: Consultancy; Disc Medicine: Consultancy; Celgene/Bristol Myers Squibb: Consultancy; CTI BioPharma: Consultancy; Kartos Therapeutics: Consultancy; Novartis: Consultancy. Kuykendall: Novartis: Research Funding; PharmaEssentia: Honoraria; Incyte: Honoraria; Protagonist Therapeutics: Honoraria, Research Funding. Patriarca: Sobi: Consultancy, Honoraria, Other: Sobi Hospitality at ASH 2023; Sanofi: Consultancy, Honoraria, Other: Sanofi Hospitality at EHA 2022; Sanofi Hospitality at EHA 2021; Pfizer: Honoraria; Incyte: Honoraria; Alexion: Honoraria, Other: Alexion Hospitality at ASH 2022; Takeda: Honoraria; Novartis: Honoraria; BMS: Honoraria. Mesa: MorphoSys: Consultancy, Research Funding; Telios: Consultancy, Honoraria; Sierra: Consultancy, Honoraria, Research Funding; Novartis: Consultancy, Honoraria; Incyte: Consultancy, Honoraria, Research Funding; GlaxoSmithKline: Consultancy, Honoraria; Geron: Consultancy, Honoraria; Genentech: Consultancy, Honoraria, Research Funding; CTI: Consultancy, Honoraria; Bristol Myers Squibb: Consultancy, Honoraria, Research Funding; Blueprint: Consultancy, Honoraria, Research Funding; AbbVie: Consultancy, Honoraria, Research Funding. Kiladjian: Novartis: Consultancy; GSK: Consultancy; AOP Health: Consultancy; Incyte: Membership on an entity's Board of Directors or advisory committees; Abbvie: Honoraria; PharmaEssentia: Honoraria. Talpaz: Arcus: Research Funding; BMS: Membership on an entity's Board of Directors or advisory committees, Research Funding; Imago: Membership on an entity's Board of Directors or advisory committees; KyowaKirin: Membership on an entity's Board of Directors or advisory committees; Sumitomo: Membership on an entity's Board of Directors or advisory committees; SierraOncology: Membership on an entity's Board of Directors or advisory committees; GSK: Membership on an entity's Board of Directors or advisory committees; Pfizer: Membership on an entity's Board of Directors or advisory committees. Harris: Constellation Pharmaceuticals, a MorphoSys Company: Current Employment. Kays: MorphoSys AG: Current Employment. Li: MorphoSys US Inc: Current Employment. Brown: Constellation Pharmaceuticals a MorphoSys Company: Current Employment; Pfizer: Current holder of stock options in a privately-held company; Moderna: Current holder of stock options in a privately-held company; Eli Lilly: Current holder of stock options in a privately-held company; Exelixis: Current holder of stock options in a privately-held company; MorphoSys: Current holder of stock options in a privately-held company. Jegg: MorphoSys AG: Current Employment. Harrison: BMS: Consultancy, Honoraria, Speakers Bureau; IMAGO: Consultancy, Honoraria, Speakers Bureau; Galecto: Consultancy; Geron: Consultancy; AOP: Consultancy, Honoraria, Speakers Bureau; Incyte: Consultancy, Honoraria, Other: Teaching and Speaking; Research: PI, Speakers Bureau; AbbVie: Consultancy, Honoraria, Other: Teaching and speaking; Research: PI, Speakers Bureau; MSD: Consultancy, Honoraria, Speakers Bureau; Sobi: Consultancy; Janssen: Consultancy; CTI: Ended employment in the past 24 months; GSK: Consultancy, Honoraria, Other: Teaching and speaking; Research: PI, Research Funding, Speakers Bureau; MorphoSys/Constellation: Consultancy, Honoraria, Other: Research: PI, Research Funding, Speakers Bureau; Keros: Consultancy, Honoraria, Speakers Bureau; Novartis: Consultancy, Honoraria, Other: Teaching and speaking; Research: PI, Research Funding, Speakers Bureau; MPN voice: Other: Leadership role. Rampal: Zentalis: Consultancy, Research Funding; Jubilant: Consultancy; Constellation/MorphoSys: Consultancy, Research Funding; Sierra Oncology/GSK: Consultancy; Protagonist: Consultancy; Cogent: Consultancy; Sumitomo Dainippon: Consultancy; Kartos: Consultancy; Karyopharm: Consultancy; Ryvu: Research Funding; Disc Medicine: Consultancy; Galecto: Consultancy; Servier: Consultancy; CTI BioPharma: Consultancy; Stemline Therapeutics: Consultancy, Research Funding; PharmaEssentia: Consultancy; AbbVie: Consultancy; Blueprint: Consultancy; Celgene/BMS: Consultancy; Incyte Corporation: Consultancy, Research Funding; Jazz Pharmaceuticals: Consultancy; Novartis: Consultancy; Promedior: Consultancy.

*signifies non-member of ASH