Tecelra

Q: What are the side effects of Tecelra?

Most common adverse reactions (≥ 20%) were, cytokine release syndrome, nausea, fatigue, musculoskeletal pain, infections, pyrexia, constipation, vomiting, headache, diarrhea, cough, tachycardia, edema, dyspnea, and rash. ( 6.1 ) Grade 3 or 4 laboratory abnormalities (≥20%) were lymphocyte count decreased, white blood cell count decreased, neutrophil count decreased and red blood cell count… See the full label for the complete list.

Q: Who makes Tecelra?

Tecelra is listed by 1 labeler in the FDA NDC directory, including USWM CT, LLC.

afamitresgene autoleucel · Injection, Suspension · Intravenous

Prescription (Rx)

Boxed warning. WARNING: CYTOKINE RELEASE SYNDROME Cytokine Release Syndrome (CRS), which may be severe or life-threatening, occurred in patients receiving TECELRA. At the first sign of CRS, immediately evaluate patient for hospitalization and institute treatment with supportive care. Ensure that healthcare providers administering TECELRA have immediate access to medications and resuscitative equipment to manage CRS [see Preparation and Administration (2.2) , and Warnings and Precautions (5.1) ] . WARNING: CYTOKINE RELEASE SYNDROME See full prescribing information for complete boxed warning. Cytokine Release Syndrome (CRS), which may be severe or life-threatening, occurred in patients receiving TECELRA. At the first sign of CRS, immediately evaluate patient for hospitalization and institute treatment with supportive care. Ensure that healthcare providers administering TECELRA have immediate access to…

Uses

1 INDICATIONS AND USAGE TECELRA is indicated for the treatment of adults and pediatric patients 12 years of age and older with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A*02:01P, -A*02:02P, -A*02:03P, or -A*02:06P positive and whose tumor expresses the MAGE-A4 antigen as determined by FDA-approved or cleared companion diagnostic devices. TECELRA is a melanoma-associated antigen A4 (MAGE-A4)-directed genetically modified autologous T cell immunotherapy indicated for the treatment of adults and pediatric patients 12 years of age and older with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A*02:01P, -A*02:02P, -A*02:03P, or -A*02:06P positive and whose tumor expresses the MAGE-A4 antigen as determined by FDA-approved or cleared companion diagnostic devices.

Dosage and administration

For autologous use only. For intravenous use only. For autologous use only. For intravenous use only. Prior to infusion Verify patient's identity prior to infusion ( 2.2 ). Administer a lymphodepleting regimen of cyclophosphamide and fludarabine ( 2.2 ). Premedicate with acetaminophen and an H1-antihistamine ( 2.2 ). TECELRA Dose and Administration The recommended dose is between 1.62 × 10 9 to 10 × 10 9 MAGE-A4 T cell receptor (TCR) positive T cells ( 2.1 ). Administer each infusion bag within one hour of thawing. DO NOT USE a leukodepleting filter ( 2.2 ). DO NOT USE prophylactic systemic corticosteroids ( 2.2 ). 2.1 Recommended Dose The recommended dose is between 1.62 × 10 9 to 10 × 10 9 MAGE-A4 T cell receptor (TCR) positive T cells administered as a single intravenous infusion. TECELRA is provided as a single dose for infusion in one or more infusion bag(s). Verify the number of bags received for the indicated dose prior to preparation for infusion. 2.2 Preparation and Administration Receipt of TECELRA Plan for TECELRA to arrive prior to beginning lymphodepleting chemotherapy. Ensure storage conditions in vapor phase of liquid nitrogen (≤ -130°C). TECELRA is shipped directly to the healthcare facility in the vapor phase of a liquid nitrogen shipper. Upon receipt of TECELRA confirm the patient's identifiers on the metal cassette and product bag. Inspect the product for obvious signs of damage and contact 1-855-246-9232 if any anomalies are identified at the time of receipt. Transfer TECELRA in the original packaging, containing the cassette(s) protecting the infusion bag(s), to onsite storage at ≤ -130°C before the shipper expires. Store TECELRA in a manner that is consistent with How Supplied/Storage and Handling (16) . If unforeseen circumstances prevent proper storage of TECELRA consistent with How Supplied/Storage and Handling (16) , contact 1-855-246-9232 to arrange for return shipment. Preparing Patient for TECELRA Administration Pretreatment Confirm availability of TECELRA at the healthcare facility prior to starting the lymphodepleting chemotherapy regimen. Match the patient's identity with the patient identifiers on the TECELRA cassette(s) and infusion bag(s). Do not infuse TECELRA if the information on the patient-specific label(s) does not match the intended patient. Administer a lymphodepleting chemotherapy regimen of fludarabine 30 mg/m 2 /day intravenously for 4 days starting on the seventh day before TECELRA infusion (Day-7 to Day -4) and cyclophosphamide 600 mg/m 2 /day intravenously for 3 days starting the seventh day before TECELRA infusion (Day -7 to Day -5). Refer to fludarabine prescribing for information on fludarabine dosage in patients with renal impairment. Short-acting or pegylated granulocyte-colony stimulating factor (G-CSF) may be administered at the discretion of the physician, and according with institutional standards, from 24 hours after last day of lymphodepleting chemotherapy (from Day -3) until resolution of neutropenia. Premedication Premedicate with an H1-antihistamine and acetaminophen according to institutional standard practice, approximately 30-60 minutes prior to TECELRA infusion. Avoid prophylactic systemic corticosteroids, as it may interfere with the activity of TECELRA. Preparation of TECELRA for Administration Do not thaw the product until it is ready to be used. Coordinate the timing of TECELRA thaw and infusion. Confirm infusion time in advance and adjust the start time of TECELRA thaw such that it will be available for infusion when the patient is ready. A TECELRA dose may be contained in one or more infusion bag(s). Verify the number of bags received for the indicated dose prior to preparation of TECELRA for infusion. If more than one bag will be infused for the treatment dose, thaw and administer the contents of each infusion bag completely before proceeding to thaw and infuse the contents of the next infusion bag. 1. Confirm patient identity. Prior to TECELRA preparation, match the patient's identity with the patient identifiers on each TECELRA cassette. Do not remove the TECELRA infusion bag(s) from the cassette(s) if the information on the patient-specific label does not match the patient's identity. Contact 1-855-246-9232 if there are any discrepancies between the labels and the patient identifiers. 2. Once patient identity is confirmed, remove TECELRA infusion bag(s) from the cassette(s) and check that the patient identifiers on the cassette label match the patient identifiers on the bag label. Contact 1-855-246-9232 if there are any discrepancies between the patient identifiers on the cassette and bag labels. 3. Inspect the infusion bag for any breaches of container integrity such as breaks or cracks before thawing. If the bag is compromised, do not infuse the contents and call 1-855-246-9232. 4. Place the infusion bag inside a second sealable, preferably sterile bag per institutional standard practice. 5. Thaw the infusion bag at approximately 37°C using a water bath or dry thaw method, until there is no visible ice in the infusion bag. 6. Gently mix the contents of the bag by massaging, to disperse visible cell clumps. Small clumps of cellular material should disperse with gentle manual massaging. Do not infuse TECELRA if clumps are not dispersed. Call 1-855-246-9232. 7. Keep TECELRA at ambient temperature (20°C to 25°C) once thawed. Do not pre-filter into a different container, wash, spin down, or resuspend TECELRA in new media prior to infusion. 8. Administer within one hour. TECELRA Administration 9. Do not use a leukodepleting filter. 10. Follow universal precautions and local biosafety guidelines for handling and disposal of TECELRA to avoid potential transmission of infectious diseases, due to the presence of human blood cells that are genetically modified with replication incompetent, self-inactivating lentiviral vector. 11. Confirm patient identity with the patient identifiers on the infusion bag(s).

Dosage forms and strengths

3 DOSAGE FORMS AND STRENGTHS TECELRA is a cell suspension for intravenous infusion. A single dose of TECELRA contains 1.62 × 10 9 to 10 × 10 9 MAGE-A4 TCR positive T cells in one or more infusion bag(s) [see How Supplied/Storage and Handling (16) , Dosage and Administration (2.1) ]. TECELRA is A cell suspension for intravenous infusion. Provided in one or more infusion bag(s) containing 1.62 × 10 9 to 10 × 10 9 MAGE-A4 TCR positive T cells ( 3 ).

Contraindications

4 CONTRAINDICATIONS DO NOT use TECELRA in patients who are heterozygous or homozygous for HLA-A*02:05P. DO NOT use TECELRA in patients who are heterozygous or homozygous for HLA-A*02:05P ( 4 ).

Warnings and precautions

Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS): Monitor for ICANS events for at least 2 weeks after treatment with TECELRA. Effects on Ability to Drive and Use Machines: Advise patients to refrain from driving and engaging in hazardous occupations or activities, such as operating heavy or potentially dangerous machinery, for at least 2 weeks after receiving TECELRA ( 5.2 ). Prolonged Severe Cytopenia: Patients may exhibit severe cytopenia (hemoglobin < 8.0 g/dL, neutrophils < 1,000/mm 3 , platelets < 50,000/mm 3 ) for several weeks following lymphodepleting chemotherapy and TECELRA infusion. Monitor blood counts prior to and after TECELRA infusion ( 5.3 ). Infections: Monitor patients for signs and symptoms of infection; treat appropriately ( 5.4 ). Secondary Malignancies: In the event that a secondary malignancy occurs after treatment with TECELRA, contact 1-855-246-9232 ( 5.5 ). Hypersensitivity Reactions: Monitor for hypersensitivity reactions during infusion ( 5.6 ). 5.1 Cytokine Release Syndrome Cytokine release syndrome (CRS), including potentially life-threatening reaction has been observed following administration of TECELRA. CRS occurred in 72% of patients, including Grade ≥ 3 CRS in 2% patients. The median time to onset was 2 days (range: 1 to 7 days) and the median time to resolution was 3 days (range: 1 to 14 days). The most common symptoms were fever (97%), tachycardia (58%), hypotension (31%), nausea/vomiting (26%) and headache (21%) [see Adverse Reactions (6) ] . Management for CRS (including Grade 1) was tocilizumab (40%) and siltuximab (1 patient). Eight participants also required corticosteroids for CRS management. Ensure that healthcare providers administering TECELRA have immediate access to medications and resuscitative equipment to manage CRS. Ensure patients are euvolemic prior to initiating the infusions. During and following TECELRA administration, closely monitor patients for signs and symptoms of CRS. Following treatment with TECELRA, monitor patients for at least 7 days at the healthcare facility for CRS. Continue to monitor patients for CRS for at least 2 weeks following treatment with TECELRA. Counsel patients to seek medical attention should signs or symptoms of CRS occur. At the first sign of CRS, immediately evaluate patient for hospitalization and institute treatment with supportive care based on severity and consider further management per current practice guidelines. 5.2 Immune Effector Cell-associated Neurotoxicity Syndrome Immune Effector Cell-associated Neurotoxicity Syndrome (ICANS) has been observed following administration of TECELRA. Six patients (4%) had ICANS; five Grade 1 and one Grade 2. Time to onset was 2 to 8 days and time to resolution was 1 to 7 days. Symptoms included mild mental status changes. Other symptoms may include disorientation to time and place, mild drowsiness, mild inattention. Severe symptoms may include altered level of consciousness, seizures, cerebral edema, impairment of cognitive skills, progressive aphasia, motor weakness. Ensure that healthcare providers administering TECELRA have immediate access to medications and resuscitative equipment to manage ICANS. During and following TECELRA administration, closely monitor patients for signs and symptoms of ICANS. Following treatment with TECELRA, monitor patients for at least 7 days at the healthcare facility for ICANS. Continue to monitor patients for ICANS for at least 2 weeks following treatment with TECELRA. Counsel patients to seek medical attention should signs or symptoms of ICANS occur. At the first sign of ICANS, immediately evaluate patients for hospitalization and institute treatment with supportive care based on severity and consider further management per current practice guidelines. Effect on Ability to Drive and Use Machines Due to the potential for neurologic events, including dizziness and presyncope, patients receiving TECELRA are at risk for altered or decreased coordination in the 2 weeks following infusion. Advise patients to refrain from driving and engaging in hazardous occupations or activities, such as operating heavy or potentially dangerous machinery, during this initial period. 5.3 Prolonged Severe Cytopenia Patients may exhibit severe cytopenias, including neutropenia and thrombocytopenia [see Adverse Reactions (6) ] . Patients exhibited anemia, neutropenia, and/or thrombocytopenia for several weeks following lymphodepleting chemotherapy and TECELRA infusion. Patients with Grade ≥ 3 cytopenia not resolved by week 4 included neutropenia (11%), anemia (6%), and thrombocytopenia (5%). The median time to resolution was 7.0 weeks (range: 6.1 to 12.4 weeks) for neutropenia, 6.4 weeks (range: 5.3 to 12.1 weeks) for anemia, and 9 weeks (range: 5.3 to 12.1 weeks) for thrombocytopenia. Monitor blood counts after TECELRA infusion. Manage cytopenia with growth factor and blood product transfusion according to local institutional guidelines/clinical practice. 5.4 Infections Infections may occur following lymphodepleting chemotherapy and TECELRA infusion. Infections (all grades) occurred in 35% of patients with synovial sarcoma. Grade 3 or higher infections occurred in 12% of patients. Do not administer TECELRA to patients with active infections and/or inflammatory disorders. Monitor patients for signs and symptoms of infection before and after TECELRA infusion and treat patients appropriately. Febrile neutropenia was observed in 10% of patients after TECELRA infusion and may be concurrent with CRS. In the event of febrile neutropenia, evaluate for infection and manage with broad-spectrum antibiotics, fluids and other supportive care, as medically indicated. Viral reactivation has occurred in patients following treatment with TECELRA. Perform screening for Epstein-Barr Virus, Cytomegalovirus, Hepatitis B Virus, Hepatitis C Virus, Human Immunodeficiency Virus, and any other infectious agents if clinically indicated.

Side effects

Most common adverse reactions (≥ 20%) were, cytokine release syndrome, nausea, fatigue, musculoskeletal pain, infections, pyrexia, constipation, vomiting, headache, diarrhea, cough, tachycardia, edema, dyspnea, and rash. ( 6.1 ) Grade 3 or 4 laboratory abnormalities (≥20%) were lymphocyte count decreased, white blood cell count decreased, neutrophil count decreased and red blood cell count decreased ( 6.1 ). The most common serious adverse reactions (≥ 5%) were cytokine release syndrome and infections ( 6.1 ). To report SUSPECTED ADVERSE REACTIONS, contact USWM CT, LLC at 1-855-246-9232 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The safety of TECELRA was evaluated in the SPEARHEAD-1 study (Cohorts 1, 2, 3) in which 137 patients with advanced synovial sarcoma received TECELRA across a dose of 1.01 × 10 9 to 10 × 10 9 MAGE-A4 TCR positive T cells [see Clinical Studies (14) ]. Serious adverse reactions occurred in 35% of patients with synovial sarcoma. The most common serious adverse reactions (occurring in ≥ 5%) were CRS (7%) and infections (8%). Table 1 summarizes adverse reactions that occurred in at least 10% of patients. Table 1. Adverse Reactions Occurring in ≥10% of Patients in SPEARHEAD-1 (Cohorts 1, 2, 3) SOC Grouped Term (N=137) All Grades n (%) Grade ≥ 3 n (%) a Includes all adverse reactions reported following lymphodepleting chemotherapy and TECELRA, regardless of attribution to TECELRA Gastrointestinal disorders Nausea 88 (64) 5 (4) Vomiting 38 (28) 2 (2) Constipation 40 (29) 1 (1) Diarrhea 34 (25) 0 (0) Abdominal pain Is a composite that includes multiple related terms. 25 (18) 5 (4) General disorders and administration site conditions Fatigue 72 (53) 2 (2) Pyrexia 41 (30) 5 (4) Edema Edema includes ascites, fluid retention, hypervolemia, edema peripheral, pleural effusion, face edema, localized edema, peripheral swelling, and swelling. 29 (21) 3 (2) Chills 21 (15) 0 (0) Immune system disorders Cytokine Release Syndrome As per American Society for Transplantation and Cellular Therapy (ASTCT) criteria 1 98 (72) 3 (2) Infections and infestations Any infection Any infection includes all infection terms under the 'Infections and infestations' System Organ Class 48 (35) 16 (12) Nervous system disorders Headache 36 (26) 2 (2) Dizziness 22 (16) 0 (0) Encephalopathy Encephalopathy includes confusional state, dysgeusia, cognitive disorder, somnolence, aphasia, dysarthria, and amnesia. 17 (12) 0 (0) Neuropathy peripheral 14 (10) 0 (0) Metabolism and nutrition disorders Decreased appetite 25 (18) 3 (2) Musculoskeletal and connective tissue disorders Musculoskeletal pain 60 (44) 5 (4) Respiratory, thoracic, and mediastinal disorders Cough 34 (25) 0 (0) Dyspnea 27 (20) 5 (4) Renal and urinary disorders Renal insufficiency 15 (11) 1 (1) Vascular disorders Hemorrhage 26 (19) 2 (2) Hypotension 25 (18) 2 (2) Hypertension 15 (11) 3 (2) Cardiac disorders Tachycardia 30 (22) 0 (0) Skin and subcutaneous tissue disorders Rash 28 (20) 3 (2) Alopecia 17 (12) 0 (0) Psychiatric disorders Insomnia 16 (12) 0 (0) Other clinically important adverse reactions occurring in patients receiving TECELRA include Grade 1 and Grade 2 ICANS reported in six patients (4%). Table 2. Laboratory Abnormalities Abnormalities are laboratory values that were considered an adverse event Worsened from Baseline in ≥10% of Patients in SPEARHEAD-1 (Cohorts 1, 2, 3) N=137 Laboratory Abnormalities All Grades n (%) Grade 3 or 4 n (%) Grading based on NCI CTCAE version 5.0. Lymphocyte count decreased 137 (100) 137 (100) Neutrophil count decreased 132 (96) 122 (89) White blood cell decreased 134 (98) 121 (88) Red blood cell decreased 130 (95) 33 (24) Platelet count decreased 118 (86) 25 (18) Aspartate aminotransferase increased 82 (60) 8 (6) Alanine aminotransferase increased 64 (47) 8 (6)

Drug interactions

None

Use in specific populations

8.1 Pregnancy Risk Summary There are limited available data with TECELRA use in pregnant women. In the SPEARHEAD-1 clinical trial, there were two pregnancies in patients treated with TECELRA. One patient became pregnant 6 months following treatment with TECELRA and the outcome of this pregnancy was premature birth (30 weeks gestation) with healthy infant. A second patient was found to be pregnant two months following treatment with TECELRA and the pregnancy was electively terminated. No animal reproductive and developmental toxicity studies have been conducted with TECELRA to assess whether it can cause fetal harm when administered to a pregnant woman. It is not known if TECELRA has the potential to be transferred to the fetus and cause fetal toxicity. Therefore, TECELRA is not recommended for women who are pregnant, and pregnancy after TECELRA administration should be discussed with the treating physician. Report all pregnancies following treatment with TECELRA to 1-855-246-9232. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2-4% and 15-20%, respectively. 8.2 Lactation Risk Summary There is no information regarding the presence of TECELRA in human milk, the effect on the breastfed infant, and the effects on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for TECELRA and any potential adverse effects on the breastfed infant from TECELRA or from the underlying maternal condition. 8.3 Females and Males of Reproductive Potential Pregnancy Testing Verify pregnancy status of females with reproductive potential prior to starting treatment with TECELRA. Contraception See the Prescribing Information for fludarabine and cyclophosphamide for information on the need for effective contraception in patients who receive the lymphodepleting chemotherapy. There are insufficient exposure data to provide a recommendation concerning duration of contraception following treatment with TECELRA. Infertility There are no data on the effects of TECELRA on human fertility. 8.4 Pediatric Use The safety and effectiveness of TECELRA have been established in pediatric patients 12 years and older. Use of TECELRA is supported by a single arm trial of TECELRA (SPEARHEAD-1) in adults and pediatric patients 12 years and older, which enrolled 6 pediatric patients aged 13 years to less than 17 years. TECELRA exposure in pediatric patients 12 years and older is comparable to that of adults and the courses of unresectable or metastatic synovial sarcoma is sufficiently similar in pediatric patients aged 12 years and older to that of adults to allow extrapolation of safety and efficacy. [ See Adverse Reactions (6.1) , Clinical Pharmacology (12) , and Clinical Studies (14) ] The safety and effectiveness of TECELRA in pediatric patients aged less than 12 years have not been established. 8.5 Geriatric Use Of the 137 patients with synovial sarcoma in the SPEARHEAD-1 study that received TECELRA, 5.8% were 65 years of age or older. Clinical studies of TECELRA did not include sufficient numbers of patients aged 65 and over to conclude whether they respond differently from younger patients.

Pregnancy

Pediatric use

8.4 Pediatric Use The safety and effectiveness of TECELRA have been established in pediatric patients 12 years and older. Use of TECELRA is supported by a single arm trial of TECELRA (SPEARHEAD-1) in adults and pediatric patients 12 years and older, which enrolled 6 pediatric patients aged 13 years to less than 17 years. TECELRA exposure in pediatric patients 12 years and older is comparable to that of adults and the courses of unresectable or metastatic synovial sarcoma is sufficiently similar in pediatric patients aged 12 years and older to that of adults to allow extrapolation of safety and efficacy. [ See Adverse Reactions (6.1) , Clinical Pharmacology (12) , and Clinical Studies (14) ] The safety and effectiveness of TECELRA in pediatric patients aged less than 12 years have not been established.

Geriatric use

8.5 Geriatric Use Of the 137 patients with synovial sarcoma in the SPEARHEAD-1 study that received TECELRA, 5.8% were 65 years of age or older. Clinical studies of TECELRA did not include sufficient numbers of patients aged 65 and over to conclude whether they respond differently from younger patients.

Description

(afamitresgene autoleucel) is a melanoma-associated antigen A4 (MAGE-A4)-directed genetically modified autologous T cell immunotherapy product consisting of CD4 and CD8 positive T cells transduced with a self-inactivating lentiviral vector (LV) expressing an affinity-enhanced T cell receptor (TCR) specific for the human MAGE-A4. Autologous T cells transduced with MAGE-A4-c1032 LV express the affinity-enhanced TCR on the cell surface. The TCR recognizes an HLA-A*02 restricted MAGE-A4 peptide. MAGE-A4 is an intracellular cancer-testis antigen that has restricted expression in normal tissues and is expressed in synovial sarcoma. TECELRA is prepared from the patient's peripheral blood mononuclear cells (PBMCs), which are obtained via a standard leukapheresis procedure. The PBMCs are enriched for T cells and are then transduced with a replication-incompetent LV containing the MAGE-A4 TCR transgene. The transduced T cells are expanded, washed, formulated into a suspension, and cryopreserved. The product must pass a sterility test before release and shipping as a frozen suspension in one or more infusion bag(s). The product is thawed prior to infusion back into the patient [see Preparation and Administration (2.2) , How Supplied/Storage and Handling (16) ]. The drug product formulation contains 5% dimethyl sulfoxide (DMSO).

Mechanism of action

12.1 Mechanism of Action TECELRA is a genetically modified autologous T cell immunotherapy consisting of CD4 and CD8 positive T cells transduced with a self-inactivating LV to express an affinity-enhanced TCR specific for human MAGE-A4 on the cell surface. The TCR recognizes an HLA-A*02 restricted MAGE-A4 peptide. MAGE-A4 is an intracellular cancer-testis antigen that has restricted expression in normal tissues and is expressed in synovial sarcoma. Antigen-specific activation of TECELRA via TCR-peptide-HLA-A*02 complex results in T cell proliferation, cytokine secretion, and killing of MAGE-A4/HLA-A*02 expressing synovial sarcoma cells.

How supplied

16 HOW SUPPLIED/STORAGE AND HANDLING TECELRA is supplied in one or more infusion bag(s) containing a frozen suspension of genetically modified autologous T cells in 5% DMSO. Each TECELRA infusion bag is individually packed in a metal cassette. Product and patient-specific labels are located on both the product infusion bag(s) and the protective shipping cassette(s). Each infusion bag (250ml) is contained within a protective metal cassette (NDC 83205-0001-2). TECELRA is shipped in a liquid nitrogen dry vapor shipper at less than or equal to -130°C. Store TECELRA in the original packaging, containing the cassette(s) protecting the infusion bag(s), in the vapor phase of liquid nitrogen at less than or equal to -130°C.

Storage

TECELRA is shipped in a liquid nitrogen dry vapor shipper at less than or equal to -130°C. Store TECELRA in the original packaging, containing the cassette(s) protecting the infusion bag(s), in the vapor phase of liquid nitrogen at less than or equal to -130°C.

Patient information

Advise the patient to read the FDA-approved patient labeling (Medication Guide). Discuss the following with the patient: Inform patients that there is a chance of manufacturing or shipping failure (approximately 7% in the clinical trial). Therefore, a second manufacture of TECELRA may be attempted. Inform patients that additional therapy (other than lymphodepletion) may be necessary before TECELRA manufacturing is completed. This may increase the risk of adverse reactions during the pre-infusion period, which could delay or prevent administration of TECELRA. Inform patients that following infusion, it will be necessary to be monitored daily at the healthcare facility for at least 7 days for signs and symptoms of cytokine release syndrome (CRS). Patients must remain within proximity of a healthcare facility for at least 2 weeks following infusion. Advise patients to seek immediate medical attention if any of the following occur: Cytokine Release Syndrome : inform patients that symptoms may include fever, rigors, fast heartbeat, irregular heartbeat, low blood pressure, lightheadedness or dizziness, shortness of breath, nausea/vomiting, diarrhea, and headache [see Warnings and Precautions (5.1) and Adverse Reactions (6) ]. Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS) : inform patients that symptoms may include confusion, depressed level of consciousness, delirium, seizures, language difficulty [see Warnings and Precautions (5.2) and Adverse Reactions (6) ]. Bone marrow suppression and prolonged severe cytopenias : inform patients that symptoms may include bleeding or bruising, tiredness, shortness of breath, fever, pain, redness for several weeks following lymphodepleting chemotherapy and TECELRA blood counts before and after TECELRA infusion should be periodically monitored [see Warnings and Precautions (5.3) and Adverse Reactions (6) ]. Infections : inform patients that they may exhibit signs or symptoms associated with infection, and that past infections can be reactivated following treatment with TECELRA [see Warnings and Precautions (5.4) and Adverse Reactions (6) ]. Advise patients for the need to: Contact 1-855-246-9232 if they are diagnosed with a secondary malignancy [see Warnings and Precautions (5.5) ]. Refrain from driving or operating heavy or potentially dangerous machines for at least 2 weeks after TECELRA administration [see Warnings and Precautions (5.2) ].

Label text from the FDA structured product label by USWM CT, LLC (revised Jul 15, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Afamitresgene Autoleucel in 1 product

Tecelra NDC products (1)

NDC	Strength & form	Labeler	Type
83205-0001	Afamitresgene Autoleucel 10000000000 1/1 Injection, Suspension	USWM CT, LLC	BLA

Frequently asked questions

What is Tecelra used for?

What are the side effects of Tecelra?

Who makes Tecelra?

Tecelra is listed by 1 labeler in the FDA NDC directory, including USWM CT, LLC.