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Arcellx

Arcellx logo
🇺🇸United States
Ownership
Public
Established
2015-01-01
Employees
130
Market Cap
$3.8B
Website
http://www.arcellx.com
Introduction

Arcellx, Inc is a clinical-stage biotechnology company, which provides cell therapy through the development of innovative immunotherapies for patients with cancer and other incurable diseases. The company was founded by David M. Hilbert and Luba Zaritskaya in December 2014 and is headquartered in Gaithersburg, MD.

Clinical Trials

2

Active:0
Completed:0

Trial Phases

1 Phases

Phase 1:2

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials

Phase 1
2 (100.0%)

A Phase 1 Study of Anitocabtagene Autoleucel for the Treatment of Subjects With Non-oncology Plasma Cell-related Diseases

Phase 1
Recruiting
Conditions
Muscular Diseases
Neuromuscular Manifestations
Autoimmune
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Myasthenia Gravis
Muscle Weakness
Interventions
Biological: anito-cel
Drug: Standard Lymphodepletion regimen
First Posted Date
2024-10-04
Last Posted Date
2025-01-13
Lead Sponsor
Arcellx, Inc.
Target Recruit Count
30
Registration Number
NCT06626919
Locations
🇺🇸

University of California, Irvine, Orange, California, United States

Phase I Study of Cell Therapies for the Treatment of Patients With Relapsed or Refractory AML or High-risk MDS

Phase 1
Recruiting
Conditions
Acute Myeloid Leukemia
Myelodysplastic Syndromes
First Posted Date
2022-07-13
Last Posted Date
2024-06-12
Lead Sponsor
Arcellx, Inc.
Target Recruit Count
24
Registration Number
NCT05457010
Locations
🇺🇸

City of Hope, Duarte, California, United States

🇺🇸

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States

🇺🇸

Dana Farber Cancer Institute, Boston, Massachusetts, United States

and more 2 locations

News

Arcellx's Anito-cel Shows 97% Response Rate in Pivotal Multiple Myeloma Trial

Arcellx's Phase 2 iMMagine-1 study of anitocabtagene autoleucel (anito-cel) demonstrated a 97% overall response rate and 68% complete response rate in 117 patients with relapsed/refractory multiple myeloma.

CAR-T Cell Therapy Funding Surges to $141.2 Billion as Industry Expands Globally

The CAR-T cell therapy industry has raised over $141.2 billion through various financing mechanisms, with estimates suggesting total industry funding could reach $281.7 billion when including undisclosed deals.

Bristol Myers Squibb Acquires 2seventy bio for $286 Million to Gain Full Control of CAR-T Therapy Abecma

Bristol Myers Squibb has agreed to acquire 2seventy bio for $286 million, ending the profit-sharing arrangement for the BCMA-targeted CAR-T therapy Abecma used in multiple myeloma treatment.

CAR T-cell Therapy Pipeline Surges with 180+ Companies Advancing Novel Cancer Treatments

The CAR T-cell therapy pipeline has experienced significant growth, with over 180 companies actively developing more than 200 innovative cell therapy candidates across various stages of clinical development.

Anitocabtagene Autoleucel Shows Durable Efficacy in Advanced Multiple Myeloma

Anitocabtagene autoleucel (anito-cel) demonstrates a high overall response rate of 97% in heavily pretreated, high-risk relapsed or refractory multiple myeloma patients.

Global Review Highlights Clinical Trial Landscape for Relapsed Multiple Myeloma

• A comprehensive review of global clinical trials for relapsed multiple myeloma (R/R MM) reveals key trends in trial locations, phases, and sponsor types. • The analysis identifies prominent drugs under investigation and highlights recent clinical trial news, including updates from ASH 2024 and other major meetings. • The review emphasizes the importance of understanding trial enrollment trends and success rates to inform business strategies and identify key opportunities in the R/R MM therapeutics market. • Recent data showcases promising results for novel combinations and CAR-T cell therapies, suggesting potential breakthroughs in treating R/R MM.

Carvykti Shows High MRD Negativity Rates in Relapsed/Refractory Multiple Myeloma

• Carvykti (ciltacabtagene autoleucel) demonstrated an 89% minimal residual disease (MRD) negativity rate in patients with relapsed or refractory multiple myeloma after nearly three years of follow-up. • The MRD negativity rate with Carvykti was more than double that of standard therapies, showing a highly statistically significant treatment effect (p < 0.0001). • A prior data release showed Carvykti significantly increased overall survival and reduced the risk of death by 45% compared to standard therapies. • While Carvykti shows promise, emerging BCMA CAR-T therapies with potentially improved safety profiles may challenge its market share.

Arcellx's Anito-Cel Shows High Response Rate in Relapsed/Refractory Multiple Myeloma

• Arcellx's anito-cel demonstrated a 97% overall response rate and a 62% complete response rate in patients with relapsed or refractory multiple myeloma. • The iMMagine-1 Phase 2 study showed 93.1% of evaluable patients achieved minimal residual disease negativity, indicating deep remission. • No delayed neurotoxicities were observed, highlighting a favorable safety profile compared to other CAR-T therapies. • The Phase 1 study of anito-cel showed a 30.2-month median progression-free survival, suggesting long-term efficacy.

Arlo-Cel and Antio-Cel Show Promise in Relapsed/Refractory Multiple Myeloma

Arlocabtagene autoleucel (arlo-cel) demonstrated a 91% overall response rate in heavily pretreated multiple myeloma patients, regardless of high-risk cytogenetics or prior BCMA-directed therapy.

Kite Highlights CAR T-cell Therapy Portfolio with Positive Survival Outcomes at ASH 2024

• Kite, a Gilead Company, will present 18 presentations at ASH 2024, showcasing its CAR T-cell therapy portfolio across various blood cancers. • Anito-cel, co-developed with Arcellx, demonstrates durable responses in relapsed/refractory multiple myeloma patients, with a 30.2-month median progression-free survival in Phase 1. • Yescarta shows superior overall survival versus standard therapy in relapsed/refractory large B-cell lymphoma, supported by the largest real-world analysis of CAR T for second-line therapy. • Tecartus demonstrates durable responses in relapsed/refractory mantle cell lymphoma, with five-year outcomes from ZUMA-2 highlighting unprecedented efficacy three years post-approval.

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