Celularity Inc. (CELU)

US — Healthcare Sector
Peers: IMMX  ZVSA  HEPA  AVRO  EFTR  CNSP  VECT    NAVB  SONN 

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Key Metrics & Ratings

  • symbol CELU
  • Rev/Share 2.4769
  • Book/Share 0.4037
  • PB 5.5488
  • Debt/Equity 3.2854
  • CurrentRatio 0.383
  • ROIC -0.4707

 

  • MktCap 53646208.0
  • FreeCF/Share -0.2998
  • PFCF -8.1753
  • PE -0.6869
  • Debt/Assets 0.2188
  • DivYield 0
  • ROE -3.3523

 

  • Rating D+
  • Score 1
  • Recommendation Strong Sell
  • P/E Score 1
  • DCF Score 1
  • P/B Score 1
  • D/E Score 1

Recent Analyst Ratings

Type Ticker Analyst Firm Previous Rating Current Rating Previous Price Target Current Price Target Date
No ratings available.

News

Celularity Receives Nasdaq Notice Regarding Form 10-Q
CELU
Published: May 30, 2025 by: GlobeNewsWire
Sentiment: Neutral

FLORHAM PARK, N.J., May 30, 2025 (GLOBE NEWSWIRE) -- Celularity Inc. (Nasdaq: CELU) (“Celularity” or the “Company”), a cellular and regenerative medicine company, today announced that on May 28, 2025, Nasdaq notified the Company that it did not timely file its Quarterly Report on Form 10-Q for the period ended March 31, 2025. Based on this latest notice, the Company is not in compliance with Listing Rule 5250 (c)(1), which requires the Company to timely file all required periodic financial reports with the Securities and Exchange Commission.

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image for news Celularity Receives Nasdaq Notice Regarding Form 10-Q
Celularity Announces Full Year 2024 Operating and Financial Results
CELU
Published: May 09, 2025 by: GlobeNewsWire
Sentiment: Neutral

Net revenues for the year ending December 31, 2024, totaled $54.2 million, an increase of $31.4 million, or 138.1%, compared to the previous year. Net revenues for the year ending December 31, 2024, totaled $54.2 million, an increase of $31.4 million, or 138.1%, compared to the previous year.

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image for news Celularity Announces Full Year 2024 Operating and Financial Results
Celularity Receives FDA Tissue Reference Group Recommendation Letters for its Natalin and Acelagraft™ Wound Care Products
CELU
Published: February 25, 2025 by: GlobeNewsWire
Sentiment: Neutral

Natalin and Acelagraft™ are the latest additions to Celularity's portfolio of HCT/P 361 products for use in the treatment of partial and full thickness acute and chronic wounds Natalin and Acelagraft™ are the latest additions to Celularity's portfolio of HCT/P 361 products for use in the treatment of partial and full thickness acute and chronic wounds

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image for news Celularity Receives FDA Tissue Reference Group Recommendation Letters for its Natalin and Acelagraft™ Wound Care Products
Celularity Enters Strategic Collaboration Agreement with Clinical Stage Cell Therapy Company
CELU
Published: February 24, 2025 by: GlobeNewsWire
Sentiment: Neutral

FLORHAM PARK, N.J., Feb. 24, 2025 (GLOBE NEWSWIRE) -- Celularity Inc. (Nasdaq: CELU) (“Celularity” or the “Company”), a cellular and regenerative medicine company, today announced that it has entered into a Master Services Collaboration Agreement with BlueSphere Bio, Inc. (BSB) covering manufacturing activities for certain BSB cell therapy products.

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image for news Celularity Enters Strategic Collaboration Agreement with Clinical Stage Cell Therapy Company

About Celularity Inc. (CELU)

  • IPO Date 2019-08-08
  • Website https://www.celularity.com
  • Industry Biotechnology
  • CEO Dr. Robert Joseph Hariri M.D., Ph.D.
  • Employees 120

Celularity Inc., a clinical-stage biotechnology company, develops off-the-shelf placental-derived allogeneic cell therapies for the treatment of cancer, immune, and infectious diseases. It operates through three segments: Cell Therapy, Degenerative Disease, and BioBanking. The company's lead therapeutic programs include CYCART-19, a placental-derived CAR-T therapy, which is in Phase I clinical trial for the treatment of B-cell malignancies; CYNK-001, placental-derived unmodified natural killer (NK) cell that is in Phase I clinical trial to treat acute myeloid leukemia, as well as in Phase I/IIa clinical trial for the treatment of glioblastoma multiforme and COVID-19; CYNK-101, an allogeneic genetically modified NK cell, which is in Phase I clinical trial to treat HER2+ gastric and gastroesophageal cancers; APPL-001, a placenta-derived mesenchymal-like adherent stromal cell that is in a pre-clinical stage for the treatment of Crohn's disease; and PDA-002, a placenta-derived mesenchymal-like adherent stromal cell, which is in pre-clinical stage for the treatment of facioscapulohumeral muscular dystrophy. It also sells and licenses products that are used in surgical and wound care markets, such as Biovance and Interfyl; collects stem cells from umbilical cords and placentas; and provides cells storage under the LifebankUSA brand. The company was incorporated in 2016 and is headquartered in Florham Park, New Jersey.