A Phase 1, Multicenter, Open-Label, 2-Stage, Single-Arm Study to Evaluate the Safety and Tolerability of an Autologous Tumor-Infiltrating Lymphocytes (TIL) Regimen and Preliminary Antitumor Activity of TIL in Pediatric, Adolescent, and Young Adult Participants with Relapsed or Refractory Solid Tumors.

Inclusion Criteria

1. Participant is ≥ 8 kg and ≤ 21 years of age at the time of informed consent and

assent.

2. Histologically or cytologically confirmed recurrent or refractory solid tumor

(Rhabdomyosarcoma, Ewing sarcoma, primary CNS malignancies, melanoma) after standard

therapy which has failed all available curative therapy.

3. Acceptable performance status and an estimated life expectancy of > 6 months.

4. At least one resectable lesion (solitary or aggregate lesions) for TIL generation.

5. Following tumor resection for TIL generation, the participant will have at least one

remaining measurable lesion for response assessment.

6. Preplanned surgical procedure(s) will take place at least 14 days (for major

operative procedures) prior to the tumor resection.

7. All prior anticancer treatment-related AEs should be recovered, exceptions are

peripheral neuropathy, alopecia, vitiligo, or medically controlled endocrine

dysfunction.

8. Agreement to abide by the protocol indicated contraception use, including refraining

from donating sperm or eggs (ova, oocytes), as appropriate for the age and sexual

activity of pediatric, adolescent, and young adult participants and as required by

local regulations.

9. Signed informed consent and assent when applicable.

10. Written authorization for use and disclosure of protected health information.

11. Ability to adhere to the study visit schedule and other protocol requirements.

12. Acceptable hematologic parameters.

13. Adequate organ function.

14. Modified Ross criteria class 1 and an LVFS > 25% or an LVEF ≥ 50%.

15. Adequate pulmonary function.

16. Participant and/or the legal guardian who provided consent is willing for the

participant to receive optimal supportive care.

17. A legal guardian or primary caregiver must be available to help the study-site

personnel ensure follow-up and accompany the participant to the study site on each

assessment day according to the SoA.

Exclusion Criteria

1. Participant with a non-CNS tumor has symptomatic untreated brain metastases and/or

carcinomatous meningitis.

2. Participant has an active or uncontrolled intercurrent illness(es) that would pose

increased risks for study participation.

3. Participants are not eligible if they experience uncontrolled seizures.

4. Participants with history of intracranial hemorrhage/spinal cord hemorrhage.

5. Participant has active uveitis that requires active treatment.

6. Participant has significant psychiatric disease or substance abuse in the

investigator's opinion that would prevent adequate informed consent.

7. Participant has any form of primary or acquired immunodeficiency.

8. History of clinically significant chronic obstructive pulmonary disease, asthma,

interstitial lung disease, or other chronic lung disease.

9. History of hypersensitivity reaction to any components of the study intervention.

10. Any other condition that in the investigator's judgment would significantly increase

the risks of participation.

11. Any complication or delayed healing from an excisional procedure that in the

investigator's opinion would increase the risks of participation.

12. Another primary malignancy within the previous 3 years.

13. History of allogeneic cell or organ transplant.

14. Requiring systemic steroid therapy higher than the physiologic replacement dose.

15. Received or will receive a live or attenuated vaccination within 28 days prior to

the start of the NMA-LD.

16. Any active viral, bacterial, or fungal infection requiring ongoing systemic

treatment.