Iovance Biotherapeutics (Mfg)
Philadelphia, PA
29 confirmed programs
· 11 sponsors
· Last scored 2026-04-02
70.8
Signal Score
○ FDA Inspections
✓ Clinical Trials (29)
✓ SEC Filings (13)
○ Press
○ EMA GMP
○ MHRA GMP
Quick Facts: Iovance Biotherapeutics (Mfg)
- Signal Score
- 70.8/100 (as of 2026-04-02)
- Quality Compliance
- Assessment pending
- Headquarters
- Philadelphia, PA
- Modalities
- Cell Therapy
- Active Programs
- 29 confirmed from ClinicalTrials.gov across 11 sponsors
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
- Scored By
- CDMO Signal — independent CDMO intelligence platform
Signal Score & Pillar Breakdown
Quality Compliance
—
No FDA inspection records found. This CDMO may operate under a different legal name or may not have US FDA-inspected facilities.
FDA InspectionsNo US records on file
No FDA inspection records found for this manufacturer
Quality score requires FDA inspection data
Operations
74.6
29 active programs across 11 sponsors
Modalities: Cell Therapy
19 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov
29 active programs across 11 sponsors · Modalities: Cell Therapy · 19 programs in advanced phases (Phase 2/3)
Programs
29
Sponsors11
ModalitiesCell Therapy
29 active programs across 11 sponsors
Modalities: Cell Therapy
19 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov facility matching
NCT06940739
A Study to Investigate the Safety and Efficacy of IOV-3001 in...
PHASE1/PHASE2
Recruiting
View all 29 programs →
Source: ClinicalTrials.gov · Retrieved Apr 05, 2026
Financial Stability
71.0
Strong industry presence in SEC filings (852 mentions)
Multiple manufacturing risk factors in SEC filings
Source: SEC EDGAR, press monitoring
13 SEC filings with industry mentions on record
SEC Filings13 with industry mentions
Strong industry presence in SEC filings (852 mentions)
Multiple manufacturing risk factors in SEC filings
Capacity
66.0
10 facility investment mentions in SEC filings
Sites: Philadelphia, PA
Source: SEC EDGAR, press monitoring, company profiles
1 manufacturing site
10 facility investment mentions in SEC filings
Clinical Activity 29 studies
NCT07192900
Fast TILs to Treat Metastatic Cancer Patients With Pleural Disease
PHASE1
Recruiting
NCT07288073
TIL Therapy in cSCC and MCC
PHASE2
Recruiting
NCT07288203
A Study of Lifileucel (Tumor-infiltrating Lymphocytes) in Adults With...
PHASE2
Recruiting
NCT05639972
E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally...
PHASE1/PHASE2
Recruiting
NCT06940739
A Study to Investigate the Safety and Efficacy of IOV-3001 in Adults With...
PHASE1/PHASE2
Recruiting
NCT06481592
A Study of Lifileucel (Tumor-infiltrating Lymphocytes) in Adults With...
PHASE2
Recruiting
NCT06151847
Lifileucel With Reduced Dose Fludarabine/Cyclophosphamide Lymphodepletion...
PHASE2
Unknown
NCT05727904
Study to Investigate Lifileucel Regimen Plus Pembrolizumab Compared With...
PHASE3
Recruiting
NCT05686226
E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers
PHASE2
Recruiting
NCT05607095
A Study of LN-144 or LN-145 in People With Advanced Uveal Melanoma,...
PHASE1
Recruiting
NCT05483491
KK-LC-1 TCR-T Cell Therapy for Gastric, Breast, Cervical, and Lung Cancer
PHASE1
Recruiting
NCT05361174
A Study to Investigate the Efficacy and Safety of an Infusion of IOV-4001 in...
PHASE1/PHASE2
Recruiting
NCT05176470
Neoadj Admin Autologous Tumor Infiltrating Lymphocytes & Pembrolizumab for...
PHASE1
Active Not Recruiting
NCT04614103
Autologous LN-145 in Patients With Metastatic Non-Small-Cell Lung Cancer
PHASE2
Recruiting
NCT04155710
Study of Autologous Peripheral Blood Lymphocytes in the Treatment of...
PHASE1
Completed
NCT04111510
Autologous Tumor Infiltrating Lymphocytes in Patients With Pretreated...
PHASE2
Completed
NCT04052334
Lymphodepletion Plus Adoptive Cell Therapy With High Dose IL-2 in Adolescent...
PHASE1
Completed
NCT03935347
Adoptive Cell Therapy With (LN-145) in Combination With Pembrolizumab in...
PHASE2
Withdrawn
NCT03645928
Study of Autologous Tumor Infiltrating Lymphocytes in Patients With Solid Tumors
PHASE2
Recruiting
NCT03610490
Autologous Tumor Infiltrating Lymphocytes MDA-TIL in Treating Patients With...
PHASE2
Terminated
+ 9 more studies
Source: ClinicalTrials.gov · Retrieved Apr 05, 2026
Financial Intelligence
"
Iovance was founded to build upon the promise of TIL cell therapy initially developed at academic research centers, including the National Cancer Institute, or the NCI."
"Our multi-center trials, scalable manufacturing, regulatory approvals and commercial infrastructure have transformed TIL cell therapy from a research product available to only a small number of patients, into a commercially viable treatment that is accessible for thousands of cancer patients."
"
Amtagvi
®
is the first one-time, individualized T cell therapy for a solid tumor cancer and for the treatment of adult patients with previously treated advanced, or unresectable or metastatic melanoma."
"launch of Amtagvi
®
(lifileucel), the first product within its autologous TIL cell therapy platform, while also marketing Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi
®
treatment regimen and in other applications."
"Amtagvi
®
is the first and the only one-time, individualized T cell therapy to receive U.S."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute (“NCI”)."
"launch of Amtagvi
®
(lifileucel), the first product within its autologous TIL cell therapy platform, while also marketing Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi
®
treatment regimen and in other applications."
"Amtagvi
®
is the first and the only one-time, individualized T cell therapy to receive U.S."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute (“NCI”)."
"launch of Amtagvi
®
(lifileucel), the first product within its autologous TIL cell therapy platform, while also marketing Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi
®
treatment regimen and in other applications."
"Amtagvi
®
is the first and the only one-time, individualized T cell therapy to receive U.S."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute (“NCI”)."
"launch of Amtagvi
®
(lifileucel), the first product within our autologous TIL cell therapy platform, while also marketing Proleukin
®
(aldesleukin), an interleukin-2, or IL-2, product used in the Amtagvi
®
treatment regimen and in other applications."
"Amtagvi
®
is the first and the only one-time, individualized T cell therapy to receive FDA approval for a solid tumor cancer."
"Iovance was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute, or the NCI."
"launch of Amtagvi™ (lifileucel), the first product within its autologous TIL cell therapy platform, while also marketing Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi™ treatment regimen."
"Amtagvi™ is the first and the only one-time, individualized T cell therapy to receive U.S."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute (“NCI”)."
"launch of Amtagvi™ (lifileucel), the first product within its autologous TIL cell therapy platform, and Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi™ treatment regimen."
"Amtagvi™ is the first and the only one-time, individualized T cell therapy to receive U.S."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic research centers, including the National Cancer Institute (“NCI”)."
"launch of Amtagvi™ (lifileucel), the first product within its autologous TIL cell therapy platform, and Proleukin
®
(aldesleukin), an interleukin-2 (“IL-2”) product used in the Amtagvi™ treatment regimen."
"Amtagvi™ is the first and the only one-time, individualized T cell therapy to receive FDA approval for a solid tumor cancer."
"The Company was founded to build upon the promise of TIL cell therapy that was previously demonstrated in single-center clinical trials at academic centers, including the National Cancer Institute (“NCI”)."
Source: SEC EDGAR · Retrieved Apr 05, 2026
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