Viewing data from:

ZOLADEX

NDA

GOSERELIN ACETATE | N020578 | TERSERA THERAPEUTICS LLC

1 strength0 unique patents0 unique exclusivities

PTAB Proceedings

No IPR/PGR/CBM challenges found at the Patent Trial and Appeal Board

Patent Reexaminations

No ex parte or inter partes reexamination proceedings found at USPTO

Hatch-Waxman Litigation

No ANDA patent litigation cases (NOS 835) matched from PACER

Citizen Petitions

No FDA citizen petitions matched from Regulations.gov

Clinical Trials

223 trials from ClinicalTrials.gov — 17 recruiting, 30 active, 113 completed

Trial	Phase	Status	Sponsor	Enrollment	Dates
Study of Neoadjuvant PARP Inhibition Followed by Radical Prostatectomy in Patients With Unfavorable Intermediate-Risk or High-Risk Prostate Cancer With Select HRR Gene Alterations NCT05498272	Phase 2	Active	Rana McKay, MD	32	2023-02-01 → 2026-12
Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a High Gene Risk Score, The PREDICT-RT Trial NCT04513717	Phase 3	Active	NRG Oncology	2,753	2021-01-21 → 2038-12-31
A Study of Salvage Radiotherapy With or Without Enzalutamide in Recurrent Prostate Cancer Following Surgery NCT03809000	Phase 2	Active	RTOG Foundation, Inc.	188	2019-04-15 → 2029-09-15
Nivolumab + Docetaxel + ADT in mHSPC Patients With DDRD or Inflamed Tumors NCT04126070	Phase 2	Active	Xiao X. Wei, MD	47	2020-05-11 → 2026-10-30
Neoadjuvant Study Chemotherapy vs Letrozole + Abemaciclib in HR+/HER2- High/Intermediate Risk Breast Cancer Patients NCT04293393	Phase 2	Active	Spanish Breast Cancer Research Group	200	2020-10-02 → 2033-02-28
Study on the Role of Hormonal Treatment for Two Dosage Levels of Prostate Radiation Therapy Versus Prostate Radiation Therapy Alone NCT00223145	Phase 3	Active	Abdenour Nabid	600	2000-12 → 2027-12-31
Management of Castration-Resistant Prostate Cancer with Oligometastases NCT02685397	Phase 2/3	Active	Sir Mortimer B. Davis - Jewish General Hospital	102	2016-10 → 2041-08
Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatment for Patients With a Higher Gene Risk Score, The Guidance Trial NCT05050084	Phase 3	Active	NRG Oncology	2,050	2021-12-06 → 2031-11-11
[177Lu]Lu-NeoB in Combination With Ribociclib and Fulvestrant in Participants With ER+, HER2- and GRPR+ Advanced Breast Cancer NCT05870579	Phase 1	Active	Novartis Pharmaceuticals	28	2023-11-13 → 2032-05-27
Exemestane With or Without Entinostat in Treating Patients With Recurrent Hormone Receptor-Positive Breast Cancer That is Locally Advanced or Metastatic NCT02115282	Phase 3	Active	National Cancer Institute (NCI)	608	2014-03-29 → 2027-06-02

Source: ClinicalTrials.gov. Trials matched by ingredient name.

VA Federal Supply Schedule

Government-negotiated contract prices | 2 NDCs (1 FSS, 1 Big4)

Lowest Price

$1052.45

Highest Price

$1052.45

FSS NDCs

Big4 NDCs

Description	Price	Type	Vendor	Contract End
70720-0951-30ZOLADEX 10.8MG INJ,IMPLANT	$1052.45	Big4	TerSera Therapuetics, LLC	03/14/2029
70720-0951-30ZOLADEX 10.8MG INJ,IMPLANT	$1052.45	FSS	TerSera Therapuetics, LLC	03/14/2029

Source: VA Federal Supply Schedule (va.gov). Prices are government-negotiated contract prices.

API Supply Chain5 active DMFs1 inactive

3 active API suppliers hold Drug Master Files for this ingredient.

ALP PHARM BEIJING CO LTDGOSERELIN ACETATE

DMF 297132015

ASTRAZENECA PHARMACEUTICALS LPGOSERELIN ACETATE

DMF 314882017

ASTRAZENECA PHARMACEUTICALS LPGOSERELIN ACETATE IMPLANT

DMF 314892017

BACHEM AGGOSERELIN ACETATE

DMF 343632019

BACHEM AGGOSERELIN ACETATE

DMF 356892024

CHEMI SPAInactiveGOSERELIN ACETATE

DMF 177682004

Source: FDA Drug Master Files (fda.gov). Type II API DMFs matched by ingredient.

Approval Letters

16 letters from Drugs@FDA

Date	Submission	Document
May 8, 2026	SUPPL -53	View Letter (PDF)
Sep 25, 2025	SUPPL -51	View Letter (PDF)
Jun 22, 2021	SUPPL -44	View Letter (PDF)
Feb 17, 2015	SUPPL -37	View Letter (PDF)
Oct 9, 2014	SUPPL -36	View Letter (PDF)
Jun 20, 2013	SUPPL -34	View Letter (PDF)
Jun 20, 2013	SUPPL -35	View Letter (PDF)
Jan 20, 2011	SUPPL -32	View Letter (PDF)
Jan 20, 2010	SUPPL -29	View Letter (PDF)
Jan 20, 2010	SUPPL -28	View Letter (PDF)
Jan 20, 2010	SUPPL -30	View Letter (PDF)
Oct 25, 2005	SUPPL -25	View Letter (PDF)
Jun 25, 2004	SUPPL -20	View Letter (PDF)
Feb 28, 2002	SUPPL -16	View Letter (PDF)
Feb 5, 2002	SUPPL -13	View Letter (PDF)
Jul 27, 1998	SUPPL -3	View Letter (PDF)

Source: Drugs@FDA application documents.

Products (1)

#001 — EQ 10.8MG BASE

RLD

0 patents0 exclusivities▴

IMPLANT;IMPLANTATION | Approved: Jan 11, 1996

No patent or exclusivity listings for this strength.