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| Full Name:Pfizer Inc. | Industry:pharmaceuticals | CIK:78003 | Fiscal Year End:12-31 | State/Country:NEW YORK |
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Instructions
US clinical trial status
Size of symbol reflects the phase of clinical trial. E.g. Phase 3 trial has the largest size.
Shape definition
▲ Up-triangle: study first submitted.
◼ Square: study completion(actual/anticipated).
⬤ Circle: result first posted.
Color definition
▶ Green: study is ongoing.
▶ Blue: recruitment completed.
▶ Red: study aborted/terminated/withdrawn.
▶ Pink: study in abnormal state.
US FDA submission
Size of symbol reflects the type of submission. E.g. Type 1 drug has the largest size.
◆: Approved.
◆: Tentative Approval.
Drug marketing & current status
Circle bubble denotes new drug marketing. Size is determined by drug type and market(i.e. population) size. E.g. Type 1 drug marketed in US has the largest size. Drug marketed in CA has the smallest size due to small population size.
Color definition
⬤ Blue circle: drug marketed (EU,CA), FDA submission approved (US).
⬤ Cyan circle: drug approved (CA), tentative approval (US), received positive opinion (EU)
⬤ Red circle: drug marketed/approved on the corresponding day but was later withdrawn, discontinued, cancelled, or received negative opinion.
Drug marketing status change
Square bubble denotes marketing status change. Size is determined by drug type and market(i.e. population) size.
Color definition
◼ Blue square: change from other status to marketed.
◼ Cyan square: change from other status to tentative status.
◼ Red square: change from other status to abnormal or withdrawn status.
Clinical Trials Summary Statistics
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 2 | ||||||
| 2024 | |||||||
| 2023 | |||||||
| 2022 |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 28 ⬤ | 19 ⬤ | 3 ⬤ | 1009 ⬤ | 114 ⬤ | 34 | |
| 2024 | 6 ⬤ | 2 ⬤ | 3 ⬤ | 1 ⬤ | |||
| 2023 | 14 ⬤ | 3 ⬤ | 30 ⬤ | 1 | 1 | ||
| 2022 | 5 ⬤ | 5 ⬤ | 31 ⬤ | 4 ⬤ | 2 |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 8 ⬤ | 4 ⬤ | 31 ⬤ | 18 ⬤ | |||
| 2024 | |||||||
| 2023 | 3 ⬤ | 1 ⬤ | |||||
| 2022 | 3 ⬤ |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 15 ⬤ | 17 ⬤ | 443 ⬤ | 130 ⬤ | 29 | ||
| 2024 | 1 ⬤ | ||||||
| 2023 | 6 ⬤ | 1 ⬤ | 2 ⬤ | ||||
| 2022 | 6 ⬤ | 2 ⬤ | 3 ⬤ | 1 ⬤ | 1 |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 3 ⬤ | 2 ⬤ | 29 | 1 ⬤ | 5 | ||
| 2024 | |||||||
| 2023 | 1 ⬤ | ||||||
| 2022 | 2 ⬤ | 1 ⬤ |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 27 ⬤ | 32 ⬤ | 1 ⬤ | 535 ⬤ | 106 ⬤ | 12 | |
| 2024 | 1 ⬤ | ||||||
| 2023 | 9 ⬤ | 1 ⬤ | 2 ⬤ | ||||
| 2022 | 7 ⬤ | 8 ⬤ | 5 ⬤ | 2 ⬤ |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 8 ⬤ | 4 ⬤ | 229 ⬤ | 34 ⬤ | 14 ⬤ | ||
| 2024 | |||||||
| 2023 | 1 ⬤ | 1 ⬤ | |||||
| 2022 | 5 ⬤ | 2 ⬤ | 1 | 1 ⬤ |
| Year | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| ALL | 57 | 5 | 1 | ||||
| 2024 | |||||||
| 2023 | |||||||
| 2022 | 1 |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 28 ⬤ | 8 ⬤ | 15 ⬤ | 3 ⬤ | 27 ⬤ | 8 ⬤ | ||
| 2024 | 6 ⬤ | 1 ⬤ | ||||||
| 2023 | 14 ⬤ | 3 ⬤ | 6 ⬤ | 1 ⬤ | 9 ⬤ | 1 ⬤ | ||
| 2022 | 5 ⬤ | 3 ⬤ | 6 ⬤ | 2 ⬤ | 7 ⬤ | 5 ⬤ |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 19 ⬤ | 4 ⬤ | 17 ⬤ | 2 ⬤ | 32 ⬤ | 4 ⬤ | ||
| 2024 | 2 ⬤ | 1 ⬤ | ||||||
| 2023 | 3 ⬤ | 1 ⬤ | 1 ⬤ | 1 ⬤ | ||||
| 2022 | 5 ⬤ | 2 ⬤ | 8 ⬤ | 2 ⬤ |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 3 ⬤ | 1 ⬤ | ||||||
| 2024 | 3 ⬤ | |||||||
| 2023 | 1 ⬤ | |||||||
| 2022 |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 2 | 1009 ⬤ | 31 ⬤ | 443 ⬤ | 29 | 535 ⬤ | 229 ⬤ | 57 |
| 2024 | 1 ⬤ | |||||||
| 2023 | 30 ⬤ | 2 ⬤ | 2 ⬤ | |||||
| 2022 | 31 ⬤ | 3 ⬤ | 5 ⬤ | 1 | 1 |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 1 ⬤ | |||||||
| 2024 | ||||||||
| 2023 | ||||||||
| 2022 | 1 ⬤ |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 114 ⬤ | 18 ⬤ | 130 ⬤ | 5 | 106 ⬤ | 34 ⬤ | 5 | |
| 2024 | ||||||||
| 2023 | 1 | |||||||
| 2022 | 4 ⬤ | 1 ⬤ | 2 ⬤ |
| Year | Early Phase 1 | Phase 1 | Phase 1|Phase 2 | Phase 2 | Phase 2|Phase 3 | Phase 3 | Phase 4 | Others |
|---|---|---|---|---|---|---|---|---|
| ALL | 34 | 29 | 12 | 14 ⬤ | 1 | |||
| 2024 | ||||||||
| 2023 | 1 | |||||||
| 2022 | 2 | 1 | 1 ⬤ |
| Phase | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| Early Phase 1 | 2 | ||||||
| Phase 1 | 28 ⬤ | 19 ⬤ | 3 ⬤ | 1009 ⬤ | 114 ⬤ | 34 | |
| Phase 1|Phase 2 | 8 ⬤ | 4 ⬤ | 31 ⬤ | 18 ⬤ | |||
| Phase 2 | 15 ⬤ | 17 ⬤ | 443 ⬤ | 130 ⬤ | 29 | ||
| Phase 2|Phase 3 | 3 ⬤ | 2 ⬤ | 29 | 1 ⬤ | 5 | ||
| Phase 3 | 27 ⬤ | 32 ⬤ | 1 ⬤ | 535 ⬤ | 106 ⬤ | 12 | |
| Phase 4 | 8 ⬤ | 4 ⬤ | 229 ⬤ | 34 ⬤ | 14 ⬤ | ||
| Others | 57 | 5 | 1 |
| Phase | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| Early Phase 1 | |||||||
| Phase 1 | 6 ⬤ | 2 ⬤ | 3 ⬤ | 1 ⬤ | |||
| Phase 1|Phase 2 | |||||||
| Phase 2 | 1 ⬤ | ||||||
| Phase 2|Phase 3 | |||||||
| Phase 3 | 1 ⬤ | ||||||
| Phase 4 | |||||||
| Others |
| Phase | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| Early Phase 1 | |||||||
| Phase 1 | 14 ⬤ | 3 ⬤ | 30 ⬤ | 1 | 1 | ||
| Phase 1|Phase 2 | 3 ⬤ | 1 ⬤ | |||||
| Phase 2 | 6 ⬤ | 1 ⬤ | 2 ⬤ | ||||
| Phase 2|Phase 3 | 1 ⬤ | ||||||
| Phase 3 | 9 ⬤ | 1 ⬤ | 2 ⬤ | ||||
| Phase 4 | 1 ⬤ | 1 ⬤ | |||||
| Others |
| Phase | Recruiting | Active, Not Recruiting | Not Yet Recruiting | Completed | Suspended | Terminated | Withdrawn |
|---|---|---|---|---|---|---|---|
| Early Phase 1 | |||||||
| Phase 1 | 5 ⬤ | 5 ⬤ | 31 ⬤ | 4 ⬤ | 2 | ||
| Phase 1|Phase 2 | 3 ⬤ | ||||||
| Phase 2 | 6 ⬤ | 2 ⬤ | 3 ⬤ | 1 ⬤ | 1 | ||
| Phase 2|Phase 3 | 2 ⬤ | 1 ⬤ | |||||
| Phase 3 | 7 ⬤ | 8 ⬤ | 5 ⬤ | 2 ⬤ | |||
| Phase 4 | 5 ⬤ | 2 ⬤ | 1 | 1 ⬤ | |||
| Others | 1 |
Note: "Year" represents clinical trail start year determined by study first submit date.
Three grouping strategies present the same statistical data from different angles, choose any one you are comfortable with.
⬤ at least one study with latest update posted within 7 days.
⬤ at least one study with latest update posted within 30 days.
⬤ at least one study with latest update posted within 90 days.
Clinical Trials Records
| Sponsor | Overall Status | Phase | Brief Title | Disease Condition | Intervention Name | Study First Submit Date | Last Update Post Date | Results First Post Date | Completion Date | Completion Date Type | Enrollment Count |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Pfizer | Recruiting | Phase 3 | A Study to Learn About the Vaccine RSVpreF In Pregnant Participants With HIV and Their Infants | Respiratory Syncytial Virus | RSVpreF vaccine|Placebp | 2024-03-08 | 2024-04-11 | 2025-06-11 | Anticipated | 330 | |
| Pfizer | Recruiting | Phase 3 | A 52-Week Study to Learn About the Safety and Effects of Ritlecitinib in Participants With Nonsegmental Vitiligo | Vitiligo | Ritlecitinib|Ritlecitinib 100 mg|Placebo | 2023-11-30 | 2024-04-04 | 2026-08-08 | Anticipated | 400 | |
| Pfizer | Recruiting | Phase 3 | MagnetisMM-32: A Study to Learn About the Study Medicine Called Elranatamab in People With Multiple Myeloma (MM) That Has Come Back After Taking Other Treatments (Including Prior Treatment With an Anti-CD38 Antibody and Lenalidomide) | Multiple Myeloma | Elranatamab|Elotuzumab|Pomalidomide|Dexamethasone|Bortezomib|Carfilzomib | 2023-11-17 | 2024-04-11 | 2028-03-24 | Anticipated | 492 | |
| Pfizer | Recruiting | Phase 3 | A Study to Learn About the Study Medicine Called PF-07220060 in Combination With Fulvestrant in People With HR-positive, HER2-negative Advanced or Metastatic Breast Cancer Who Progressed After a Prior Line of Treatment | Advanced or Metastatic Breast Cancer | PF-07220060 CDK4 inhibitor|Fulvestrant|Everolimus|Exemestane | 2023-10-24 | 2024-04-03 | 2028-12-14 | Anticipated | 510 | |
| Pfizer | Recruiting | Phase 2|Phase 3 | A Study to Learn About the Study Medicine Sisunatovir in Adults With Respiratory Syncytial Virus (RSV) Infection | Respiratory Syncytial Virus Infection | Sisunatovir|Placebo | 2023-10-06 | 2024-04-02 | 2025-08-30 | Anticipated | 2715 | |
| Pfizer | Not yet recruiting | Phase 3 | A Study to Learn About Zavegepant as a Treatment for Multiple Migraine Attacks in Adult Participants | Migraine | Zavegepant 10 mg|Placebo - Control 1|Placebo - Control 2 | 2023-10-06 | 2024-04-25 | 2027-02-15 | Anticipated | 1280 | |
| Pfizer | Recruiting | Phase 3 | A 104-Week Study of Ritlecitinib Oral Capsules in Adults With Nonsegmental Vitiligo (Active and Stable) Tranquillo 2 | Stable Nonsegmental Vitiligo|Active Nonsegmental Vitiligo | Ritlecitinib|Ritlecitinib|Placebo | 2023-10-02 | 2024-04-11 | 2027-07-14 | Anticipated | 1450 | |
| Pfizer | Recruiting | Phase 3 | A Study to Learn About Zavegepant as the Acute Treatment of Migraine in Asian Adults | Migraine | Zavegepant|Placebo | 2023-08-03 | 2024-04-08 | 2025-09-20 | Anticipated | 1400 | |
| Pfizer | Recruiting | Phase 3 | A Study of ARV-471 (PF-07850327) Plus Palbociclib Versus Letrozole Plus Palbociclib in Participants With Estrogen Receptor Positive, Human Epidermal Growth Factor Negative Advanced Breast Cancer | Breast Cancer | ARV-471 (PF-07850327)|Palbociclib|Letrozole|Palbociclib | 2023-05-25 | 2024-04-15 | 2030-07-26 | Anticipated | 1180 | |
| Pfizer | Completed | Phase 3 | A Study to Learn About the Safety and Immune Response of 20vPnC in Adults in India. | Pneumococcal Disease | 20-valent pneumococcal conjugate vaccine | 2023-05-16 | 2024-01-16 | 2023-10-02 | Actual | 400 | |
| Pfizer | Recruiting | Phase 3 | A Study to Understand How the Study Medicine (PF-06823859) Works in People With Active Idiopathic Inflammatory Myopathies [Dermatomyositis (DM) and Polymyositis (PM)] | Myositis | PF-06823859|Placebo | 2023-04-27 | 2024-04-15 | 2025-12-04 | Anticipated | 270 | |
| Pfizer | Completed | Phase 3 | A Study to Assess the Safety, Tolerability, and Immunogenicity of RSVpreF in Adults at High Risk of Severe RSV Disease | RESPIRATORY SYNCYTIAL VIRUS (RSV) | RSVpreF|Placebo | 2023-04-24 | 2024-04-09 | 2024-03-18 | Actual | 886 | |
| Pfizer | Recruiting | Phase 3 | A Study to Learn About the Safety and Effects of Rimegepant to Prevent Migraine in Chinese Subjects. | Migraine | Rimegepant|Placebo | 2023-03-30 | 2024-04-16 | 2025-12-13 | Anticipated | 784 | |
| Pfizer | Recruiting | Phase 3 | A Study to Understand the Long-term Safety and Effects of an Experimental Gene Therapy for Duchenne Muscular Dystrophy. | Duchenne Muscular Dystrophy | fordadistrogene movaparvovec | 2023-01-09 | 2024-02-22 | 2039-05-15 | Anticipated | 250 | |
| Pfizer | Active, not recruiting | Phase 3 | A Study to Learn About the Study Medicine Etrasimod in Adults With Moderate to Severe Atopic Dermatitis (AD) Who Have Already Tried Treatments Taken by Mouth or by Injection | Atopic Dermatitis|Atopic Dermatitis, Unspecified|Eczema|Eczema, Atopic | etrasimod|Placebo | 2022-12-22 | 2024-04-02 | 2024-04-23 | Anticipated | 53 | |
| Pfizer | Active, not recruiting | Phase 3 | Safety Study of a Vaccine to Help Protect Against Lyme Disease in Healthy Children | Lyme Disease | VLA15|Normal Saline | 2022-11-22 | 2024-03-05 | 2025-06-06 | Anticipated | 3242 | |
| Pfizer | Recruiting | Phase 3 | A Study to Learn About a New Medicine Called ARV-471 (PF-07850327) in People Who Have Advanced Metastatic Breast Cancer. | Advanced Breast Cancer | ARV-471|Fulvestrant | 2022-11-16 | 2024-04-25 | 2028-05-15 | Anticipated | 560 | |
| Pfizer | Recruiting | Phase 2|Phase 3 | GBT021601-022: A Study of GBT021601 in Participants With Sickle Cell Disease (SCD) | Sickle Cell Disease | open-label GBT021601 | 2022-11-01 | 2024-04-08 | 2029-04-11 | Anticipated | 314 | |
| Pfizer | Recruiting | Phase 3 | A Clinical Trial of Study Medicine (Marstacimab) in Pediatric Patients With Hemophilia A or Hemophilia B | Hemophilia A|Hemophilia B | marstacimab | 2022-10-27 | 2024-04-01 | 2028-09-10 | Anticipated | 100 | |
| Pfizer | Recruiting | Phase 3 | A Study to Learn About the Effects of the Combination of Elranatamab (PF-06863135), Daratumumab, and Lenalidomide Compared With Daratumumab, Lenalidomide, and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma Who Are Not Candidates for Transplant | Multiple Myeloma | Elranatamab|Daratumumab|Lenalidomide|Dexamethasone | 2022-10-26 | 2024-04-16 | 2031-11-29 | Anticipated | 966 | |
| Pfizer | Recruiting | Phase 3 | A 52-Week Study of Ritlecitinib Oral Capsules in Adults and Adolescents With Nonsegmental Vitiligo (Active and Stable) Tranquillo | Stable Nonsegmental Vitiligo|Active Nonsegmental Vitiligo | Ritlecitinib|Placebo | 2022-10-06 | 2024-02-05 | 2025-06-27 | Anticipated | 600 | |
| Pfizer | Recruiting | Phase 3 | Safety and Effectiveness of Giroctocogene Fitelparvovec or Fidanacogene Elaparvovec in Patients With Hemophilia A or B Respectively | Hemophilia A|Hemophilia B | Testing of hepatic AAV Vector integration | 2022-10-03 | 2024-03-21 | 2038-01-29 | Anticipated | 263 | |
| Pfizer | Active, not recruiting | Phase 3 | Resolution of Sickle Cell Leg Ulcers With Voxelotor | Sickle Cell Disease|Leg Ulcers | Voxelotor Oral Tablet|Placebo | 2022-09-27 | 2024-04-11 | 2024-08-20 | Anticipated | 87 | |
| Pfizer | Completed | Phase 3 | A Study to Evaluate a Modified RNA Vaccine Against Influenza in Adults 18 Years of Age or Older | Influenza, Human | Quadrivalent influenza modRNA vaccine|Quadrivalent influenza vaccine | 2022-09-08 | 2024-04-03 | 2024-03-12 | Actual | 46169 | |
| Pfizer | Active, not recruiting | Phase 3 | A Study to Describe the Safety and Immunogenicity of 20vPnC in Infants in India and Taiwan | Pneumococcal Disease | 20-valent pneumococcal conjugate vaccine|13-valent pneumococcal conjugate vaccine | 2022-08-22 | 2024-03-21 | 2026-01-22 | Anticipated | 190 | |
| Pfizer | Active, not recruiting | Phase 3 | An Efficacy, Safety, Tolerability, Immunogenicity, and Lot-Consistency Clinical Trial of a 6-Valent OspA-Based Lyme Disease Vaccine (VLA15) | Lyme Disease | VLA15|Saline | 2022-07-05 | 2024-03-25 | 2025-12-26 | Anticipated | 8318 | |
| Pfizer | Recruiting | Phase 2|Phase 3 | A Phase 2/3 Study in Adult and Pediatric Participants With SCD | Sickle Cell Disease | Osivelotor | 2022-06-21 | 2024-04-08 | 2026-10-02 | Anticipated | 517 | |
| Pfizer | Completed | Phase 3 | Safety and Immunogenicity of 20vPnC in Toddlers With 2 Prior Doses of Prevenar 13 | Pneumococcal Disease | 20-valent pneumococcal conjugate vaccine|13-valent pneumococcal conjugate vaccine | 2022-06-01 | 2023-11-03 | 2023-06-01 | Actual | 356 | |
| Pfizer | Active, not recruiting | Phase 3 | Efficacy and Safety Study of Rimegepant for Migraine Prevention in Japanese Subjects (Japan Only) | Migraine | Rimegepant|Placebo | 2022-05-27 | 2024-03-04 | 2024-11-09 | Anticipated | 496 | |
| Pfizer | Completed | Phase 3 | Efficacy and Safety Study of Rimegepant for the Acute Treatment of Migraine in Japanese Subjects (Japan Only) | Migraine | Rimegepant 25 MG|Rimegepant 75 MG|Placebo | 2022-05-27 | 2024-04-11 | 2024-01-19 | Actual | 803 | |
| Pfizer | Active, not recruiting | Phase 3 | A Study to Learn About Abrocitinib Tablets in People With Atopic Dermatitis in India | Atopic Dermatitis | Abrocitinib 100 mg|Abrocitinib 200 mg | 2022-05-11 | 2023-08-01 | 2024-03-18 | Anticipated | 189 | |
| Pfizer | Recruiting | Phase 3 | A Study to Evaluate the Long-term Safety of Inclacumab Administered to Participants With Sickle Cell Disease | Sickle Cell Disease|Vaso-occlusive Crisis|Vaso-occlusive Pain Episode in Sickle Cell Disease | Inclacumab | 2022-03-29 | 2024-03-15 | 2028-11-15 | Anticipated | 520 | |
| Pfizer | Completed | Phase 3 | Long-Term Safety Study of BHV3000 for the Acute Treatment of Migraine in Chinese Subjects | Acute Migraine | Rimegepant 75mg Orally Disintegrating Tablets (ODT) | 2022-03-23 | 2024-04-11 | 2024-02-10 | Actual | 241 | |
| Pfizer | Recruiting | Phase 3 | Study With Elranatamab Versus Lenalidomide in Patients With Newly Diagnosed Multiple Myeloma After Transplant | Multiple Myeloma | Elranatamab|Lenalidomide|Lenalidomide|Elranatamab | 2022-03-18 | 2024-04-11 | 2029-10-31 | Anticipated | 760 | |
| Pfizer | Completed | Phase 3 | Safety and Immunogenicity of RSVpreF Coadministered With SIIV in Adults ≥65 Years of Age | Respiratory Syncytial Virus | RSVpreF Vaccine|Placebo|Seasonal Inactivated Influenza Vaccine | 2022-03-02 | 2023-10-27 | 2023-10-27 | 2022-10-12 | Actual | 1471 |
| Pfizer | Suspended | Phase 2|Phase 3 | EPIC-Peds: A Study to Learn About the Study Medicine Called PF-07321332 (Nirmatrelvir)/Ritonavir in Patients Under 18 Years of Age With COVID-19 That Are Not Hospitalized But Are at Risk for Severe Disease | COVID-19 | nirmatrelvir|ritonavir | 2022-02-25 | 2024-04-03 | 2027-07-03 | Anticipated | 160 | |
| Pfizer | Terminated | Phase 3 | Safety and Efficacy of BHV-3000 (Rimegepant) Orally Disintegrating Tablet for Acute Treatment of Temporomandibular Disorders | Temporomandibular Disorders (TMD) | Rimegepant|Placebo | 2022-02-21 | 2023-12-06 | 2023-05-18 | Actual | 87 | |
| Pfizer | Active, not recruiting | Phase 3 | Safety and Efficacy of BHV-3000 (Rimegepant) Orally Disintegrating Tablet for the Acute Treatment of Chronic Rhinosinusitis | Chronic Rhinosinusitis (CRS) With and Without Nasal Polyps | rimegepant 75 mg ODT|Matching placebo | 2022-01-31 | 2024-03-08 | 2024-04-10 | Anticipated | 254 | |
| Pfizer | Terminated | Phase 3 | Voxelotor Neurocognitive Function Study | Sickle Cell Disease | Voxelotor Only Product in Oral Dose Form|Placebo | 2022-01-10 | 2024-02-07 | 2022-09-30 | Actual | 1 |
Note: Use 'Search' box on top right cornor to narrow down search results. E.g. type in "phase 3" (case insensitive, with double quote) to show Phase 3 trials.
⬤ latest update posted within 7 days.
⬤ latest update posted within 30 days.
⬤ latest update posted within 90 days.
US FDA Submission Summary Statistics*
| Year | TYPE 1 | TYPE 1/4 | TYPE 2 | TYPE 3 | TYPE 3/4 | TYPE 4 | TYPE 5 | TYPE 6 | UNKNOWN |
|---|---|---|---|---|---|---|---|---|---|
| ALL | 72 | 1 | 7 | 51 | 1 | 7 | 16 | 3 | 11 |
| 2024 | |||||||||
| 2023 | 6 | ||||||||
| 2022 | 1 |
Note: "Year" determined by submission status date.
* Original submissions only. Supplementary records not counted.
⬤ at least one submission within 7 days.
⬤ at least one submission within 30 days.
⬤ at least one submission within 90 days.
US FDA Submission Records
| Sponsor | Application Type | Drug Name | Active Ingredient | Submission Code | Submission Type | Submission Status | Status Date | Application Number |
|---|---|---|---|---|---|---|---|---|
| Pfizer Inc | NDA | Talzenna | Talazoparib | Orig 1 | Approval | 2024-03-07 | 217439 | |
| Pfizer Inc | NDA | Velsipity | Etrasimod Arginine | Type 1 | Orig | Approval | 2023-10-12 | 216956 |
| Pfizer Inc | BLA | Elrexfio | Elranatamab | Type 1 | Orig | Approval | 2023-08-14 | 761345 |
| Pfizer Ireland Pharmaceuticals | BLA | Ngenla | Somatrogon Ghla | Type 1 | Orig | Approval | 2023-06-27 | 761184 |
| Pfizer | NDA | Litfulo | Ritlecitinib Tosylate | Type 1 | Orig | Approval | 2023-06-23 | 215830 |
| Pfizer | NDA | Paxlovid (Copackaged) | Nirmatrelvir; Ritonavir | Type 1 | Orig | Approval | 2023-05-25 | 217188 |
| Pfizer | NDA | Zavzpret | Zavegepant Hydrochloride | Type 1 | Orig | Approval | 2023-03-09 | 216386 |
| Pfizer | NDA | Cibinqo | Abrocitinib | Type 1 | Orig | Approval | 2022-01-14 | 213871 |
Note: Use 'Search' box on top right cornor to narrow down search results. E.g. type in "NDA" (case insensitive) to show records with "NDA" (New Drug Applications) tag.
⬤ submission status date within 7 days.
⬤ submission status date within 30 days.
⬤ submission status date within 90 days.
| Category | Sponsor | Marketing Date | Current Marketing Status | Drug Name | Active Ingredient | Submission Status Date | Submission Code | Submission Status | Marketing Status Change Date |
|---|---|---|---|---|---|---|---|---|---|
| Human Non-Bioproduct | Pfizer Inc | 2023-10-12 | Prescription | Velsipity | Etrasimod Arginine | 2023-10-12 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Inc | 2023-08-14 | Prescription | Elrexfio | Elranatamab | 2023-08-14 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Ireland Pharmaceuticals | 2023-06-27 | Prescription | Ngenla | Somatrogon Ghla | 2023-06-27 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Ireland Pharmaceuticals | 2023-06-27 | Prescription | Ngenla | Somatrogon Ghla | 2023-06-27 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2023-06-23 | Prescription | Litfulo | Ritlecitinib Tosylate | 2023-06-23 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2023-05-25 | Prescription | Paxlovid (Copackaged) | Nirmatrelvir; Ritonavir | 2023-05-25 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2023-05-25 | Prescription | Paxlovid (Copackaged) | Nirmatrelvir; Ritonavir | 2023-05-25 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2023-03-09 | Prescription | Zavzpret | Zavegepant Hydrochloride | 2023-03-09 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2022-01-14 | Prescription | Cibinqo | Abrocitinib | 2022-01-14 | Type 1 | Approval | 2022-01-25 |
| Human Non-Bioproduct | Pfizer | 2022-01-14 | Prescription | Cibinqo | Abrocitinib | 2022-01-14 | Type 1 | Approval | 2022-01-25 |
| Human Non-Bioproduct | Pfizer | 2022-01-14 | Prescription | Cibinqo | Abrocitinib | 2022-01-14 | Type 1 | Approval | 2022-01-25 |
| Human Non-Bioproduct | Pfizer | 2018-10-16 | Prescription | Talzenna | Talazoparib Tosylate | 2018-10-16 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 2018-10-16 | Prescription | Talzenna | Talazoparib Tosylate | 2018-10-16 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1999-12-28 | Discontinued | Accuretic | Hydrochlorothiazide; Quinapril Hydrochloride | 1999-12-28 | Type 4 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1999-12-28 | Discontinued | Accuretic | Hydrochlorothiazide; Quinapril Hydrochloride | 1999-12-28 | Type 4 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1999-12-28 | Discontinued | Accuretic | Hydrochlorothiazide; Quinapril Hydrochloride | 1999-12-28 | Type 4 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1994-12-22 | Prescription | Fragmin | Dalteparin Sodium | 1994-12-22 | Type 1 | Approval | 2022-03-29 |
| Human Non-Bioproduct | Pfizer Pharms | 1991-11-19 | Discontinued | Accupril | Quinapril Hydrochloride | 1991-11-19 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1991-11-19 | Discontinued | Accupril | Quinapril Hydrochloride | 1991-11-19 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1991-11-19 | Discontinued | Accupril | Quinapril Hydrochloride | 1991-11-19 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer Pharms | 1991-11-19 | Discontinued | Accupril | Quinapril Hydrochloride | 1991-11-19 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1986-12-16 | Discontinued | Calan Sr | Verapamil Hydrochloride | 1986-12-16 | Type 3 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1986-12-16 | Discontinued | Calan Sr | Verapamil Hydrochloride | 1986-12-16 | Type 3 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1984-05-08 | Discontinued | Glucotrol | Glipizide | 1984-05-08 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1984-05-08 | Discontinued | Glucotrol | Glipizide | 1984-05-08 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1963-07-18 | Discontinued | Flagyl | Metronidazole | 1963-07-18 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1963-07-18 | Discontinued | Flagyl | Metronidazole | 1963-07-18 | Type 1 | Approval | 2023-11-30 |
| Human Non-Bioproduct | Pfizer | 1961-01-27 | Discontinued | Aldactazide | Hydrochlorothiazide; Spironolactone | 1961-01-27 | Type 4 | Approval | 2023-11-30 |
| Human Bioproduct | Pfizer Ireland Pharmaceuticals | 2021-08-16 | Marketed | Ticovac | Tick Borne Encephalitis Vaccine | ||||
| Human Bioproduct | Pharmacia & Upjohn Company Llc (A Pfizer Company) | 2023-11-26 | Marketed | Atgam | Lymphocyte Immune Globulin, Anti Thymocyte Globulin (Equine) | ||||
| Human Bioproduct | Pfizer Ireland Pharmaceuticals | 2023-11-26 | Marketed | Penbraya | Meningococcal Groups A, B, C, W And Y Vaccine | ||||
| Human Bioproduct | Pfizer Inc. | 2023-11-26 | Marketed | Abrysvo | Respiratory Syncytial Virus Vaccine |
Note: This table contains human and animal drugs regulated by US FDA, and biological products regulated by CBER (Center for Biologics Evaluation and Research).
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "discontinued" (case insensitive) to show discontinued drug products.
For human non-bioproduct, marketing date was set to submission approval date.
Possible marketing statuses: Marketed, Prescription, Over-the-counter, Discontinued, None (Tentative Approval).
⬤ any of (marketing/submission/status change) within 7 days.
⬤ any of (marketing/submission/status change) within 30 days.
⬤ any of (marketing/submission/status change) within 90 days.
| Category | Sponsor | Authorization Date | Current Marketing Status | Latest Status Update | Drug Name | Active Ingredient | Withdraw Date | Opinion Date | Summary of Opinion |
|---|---|---|---|---|---|---|---|---|---|
| Human | Pfizer Europe Ma Eeig | 2023-09-15 | Authorised | 2023-09-19 | Litfulo | Ritlecitinib Tosilate | |||
| Human | Pfizer Europe Ma Eeig | 2023-08-23 | Authorised | 2023-09-15 | Abrysvo | Respiratory Syncytial Virus, Subgroup A, Stabilized Prefusion F Protein / Respiratory Syncytial Viru | |||
| Human | Pfizer Europe Ma Eeig | 2022-04-25 | Authorised | 2022-05-11 | Vydura | Rimegepant | |||
| Human | Pfizer Europe Ma Eeig | 2022-02-14 | Authorised | 2022-03-02 | Apexxnar | Pneumococcal Polysaccharide Serotype 1, Pneumococcal Polysaccharide Serotype 3, Pneumococcal Polysac | |||
| Human | Pfizer Europe Ma Eeig | 2022-02-14 | Authorised | 2022-03-02 | Ngenla | Somatrogon | |||
| Human | Pfizer Europe Ma Eeig | 2022-02-14 | Authorised | 2022-03-22 | Oxbryta | Voxelotor | |||
| Human | Pfizer Europe Ma Eeig | 2022-01-28 | Authorised | 2022-01-28 | Paxlovid | Nirmatrelvir, Ritonavir | |||
| Human | Pfizer Europe Ma Eeig | 2020-03-27 | Withdrawn | 2022-02-08 | Staquis | Crisaborole | |||
| Human | Pfizer Europe Ma Eeig | 2016-04-08 | Withdrawn | 2022-04-08 | Palonosetron Hospira | Palonosetron Hydrochloride | |||
| Human | Pfizer Europe Ma Eeig | Refused | 2022-02-15 | Raylumis | Tanezumab | ||||
| Human | Pfizer Europe Ma Eeig | Summary of Opinion | Talzenna, | Talazoparib | 2023-11-09 | Positive | |||
| Human | Pfizer Europe Ma Eeig | Summary of Opinion | Elrexfio, | Elranatamab | 2023-10-12 | Positive |
Note: This table contains human and animal drugs regulated by EMA (European Medicines Agency), and summary of opinion published by EMA based on the CHMP's or CVMP's positive or negative recommendation.
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "withdrawn" (case insensitive) to show drugs withdrawn.
Possible marketing statuses: Authorised, Refused, Withdrawn, Summary of Opinion.
Summary of Opinion: published by European Medicines Agency (EMA) based on the CHMP's or CVMP's positive or negative recommendation. Further marketing authorization is partially based on this opinion.
⬤ any of (authorization/withdrawn/opinion/status change) date within 7 days.
⬤ any of (authorization/withdrawn/opinion/status change) date within 30 days.
⬤ any of (authorization/withdrawn/opinion/status change) date within 90 days.
| Category | Sponsor | Authorization Date | Current Marketing Status | Status Date | Drug Name | Active Ingredient |
|---|---|---|---|---|---|---|
| Human | Pfizer Canada Ulc | 2004-04-08 | Cancelled Post Market | 2024-03-18 | Verapamil Hydrochloride Injection Usp | Verapamil Hydrochloride (2.5 Mg) |
| Human | Pfizer Canada Ulc | 2004-03-11 | Cancelled Post Market | 2024-03-08 | Dobutamine Injection Usp | Dobutamine (Dobutamine Hydrochloride) (250 Mg) |
| Human | Pfizer Canada Ulc | 1979-03-20 | Cancelled Post Market | 2024-03-06 | Fragmin | Dalteparin Sodium (10000 Unit) |
| Human | Pfizer Canada Ulc | 2023-11-29 | Marketed | 2024-02-13 | Litfulo | Ritlecitinib (Ritlecitinib Tosylate) (50 Mg) |
| Human | Pfizer Canada Ulc | 2024-01-31 | Approved | 2024-01-31 | Velsipity | Etrasimod (Etrasimod L Arginine) (2 Mg) |
| Human | Pfizer Canada Ulc | 2023-12-06 | Marketed | 2024-01-23 | Elrexfio | Elranatamab (44 Mg) |
| Human | Pfizer Canada Ulc | 2023-12-06 | Marketed | 2024-01-23 | Elrexfio | Elranatamab (76 Mg) |
| Human | Pfizer Canada Ulc | 2012-01-09 | Cancelled Post Market | 2024-01-09 | Vancomycin Hydrochloride For Injection, Usp | Vancomycin (Vancomycin Hydrochloride) (5 G) |
| Human | Pfizer Canada Ulc | 2012-01-09 | Cancelled Post Market | 2024-01-09 | Vancomycin Hydrochloride For Injection, Usp | Vancomycin (Vancomycin Hydrochloride) (10 G) |
| Human | Pfizer Canada Ulc | 1999-06-16 | Cancelled Post Market | 2024-01-09 | Vancomycin Hydrochloride For Injection, Usp | Vancomycin (Vancomycin Hydrochloride) (500 Mg) |
| Human | Pfizer Canada Ulc | 1999-06-16 | Cancelled Post Market | 2024-01-09 | Vancomycin Hydrochloride For Injection, Usp | Vancomycin (Vancomycin Hydrochloride) (1 G) |
| Human | Pfizer Canada Ulc | 2023-12-27 | Approved | 2023-12-27 | Beqvez | Fidanacogene Elaparvovec (10000 Bvg) |
| Human | Pfizer Canada Ulc | 2023-12-21 | Approved | 2023-12-21 | Abrysvo | Rsv Subgroup A Stabilized Prefusion F Protein (60 Mcg)|Rsv Subgroup B Stabilized Prefusion F Protein (60 Mcg) |
| Human | Pfizer Canada Ulc | 2023-12-01 | Approved | 2023-12-01 | Nurtec Odt | Rimegepant (Rimegepant Sulfate) (75 Mg) |
| Human | Pfizer Canada Ulc | 2007-03-12 | Cancelled Post Market | 2023-07-17 | Ceftriaxone Sodium For Injection Bp | Ceftriaxone (Ceftriaxone Sodium) (10 G) |
| Human | Pfizer Canada Ulc | 2006-09-20 | Cancelled Post Market | 2023-07-17 | Ceftriaxone Sodium For Injection Bp | Ceftriaxone (Ceftriaxone Sodium) (250 Mg) |
| Human | Pfizer Canada Ulc | 2004-03-04 | Cancelled Pre Market | 2023-07-17 | Ceftriaxone Sodium For Injection Bp | Ceftriaxone (Ceftriaxone Sodium) (500 Mg) |
| Human | Pfizer Canada Ulc | 2006-09-20 | Cancelled Post Market | 2023-07-17 | Ceftriaxone Sodium For Injection Bp | Ceftriaxone (Ceftriaxone Sodium) (1 G) |
| Human | Pfizer Canada Ulc | 2012-06-29 | Dormant | 2023-06-22 | Lorazepam Injection Usp | Lorazepam (4 Mg) |
| Human | Pfizer Canada Ulc | 2014-10-23 | Marketed | 2023-06-09 | Duavive | Conjugated Estrogens (0.45 Mg)|Bazedoxifene (Bazedoxifene Acetate) (20 Mg) |
| Human | Pfizer Canada Ulc | 2001-01-22 | Cancelled Post Market | 2023-04-25 | Eryc Delayed Release Capsules | Erythromycin (333 Mg) |
| Human | Pfizer Canada Ulc | 2021-01-14 | Marketed | 2023-03-13 | Abrilada | Adalimumab (20 Mg) |
| Human | Pfizer Canada Ulc | 1998-01-21 | Dormant | 2023-02-10 | Accupril 5 Mg Tab | Quinapril (Quinapril Hydrochloride) (5 Mg) |
| Human | Pfizer Canada Ulc | 2022-01-14 | Marketed | 2023-01-30 | Benvyon | Bendamustine Hydrochloride (25 Mg) |
| Human | Genmed A Division Of Pfizer Canada Ulc | 2016-08-02 | Cancelled Pre Market | 2022-12-22 | Gd Temsirolimus | Temsirolimus (25 Mg) |
| Human | Pfizer Canada Ulc | 2005-07-07 | Cancelled Post Market | 2022-10-28 | Aricept Rdt | Donepezil Hydrochloride (10 Mg) |
| Human | Pfizer Canada Ulc | 2010-08-30 | Cancelled Post Market | 2022-10-01 | Ropivacaine Hydrochloride Injection Usp | Ropivacaine Hydrochloride (5 Mg) |
| Human | Pfizer Canada Ulc | 2010-08-30 | Cancelled Post Market | 2022-10-01 | Ropivacaine Hydrochloride Injection Usp | Ropivacaine Hydrochloride (10 Mg) |
| Human | Pfizer Canada Ulc | 2008-03-27 | Cancelled Post Market | 2022-09-30 | Ciprofloxacin Injection Usp | Ciprofloxacin (2 Mg) |
| Human | Pfizer Canada Ulc | 2022-06-29 | Marketed | 2022-09-29 | Cibinqo | Abrocitinib (50 Mg) |
| Human | Pfizer Canada Ulc | 2022-06-29 | Marketed | 2022-09-29 | Cibinqo | Abrocitinib (100 Mg) |
| Human | Pfizer Canada Ulc | 2022-06-29 | Marketed | 2022-09-29 | Cibinqo | Abrocitinib (200 Mg) |
| Human | Pfizer Canada Ulc | 1997-05-29 | Cancelled Post Market | 2022-08-22 | Depo Provera | Medroxyprogesterone Acetate (150 Mg) |
| Human | Pfizer Canada Ulc | 2022-06-13 | Marketed | 2022-08-01 | Paxlovid | Ritonavir (100 Mg)|Nirmatrelvir (150 Mg) |
| Human | Pfizer Canada Ulc | 2022-05-09 | Marketed | 2022-07-08 | Prevnar 20 | Pneumococcal Polysaccharide Serotype 1 (2.2 Mcg)|Pneumococcal Polysaccharide Serotype 3 (2.2 Mcg)|Pneumococcal Polysaccharide Serotype 4 (2.2 Mcg)|Pneumococcal Polysaccharide Serotype 5 (2.2 Mcg)|Pneumococcal Polysaccharide Serotype 6 A (2.2 Mcg)|Pneumococcal Polysaccharide Serotype 6 B (4.4 Mcg)|Pneumococc |
| Human | Pfizer Canada Ulc | 2019-02-26 | Cancelled Post Market | 2022-06-09 | Vizimpro | Dacomitinib (Dacomitinib Monohydrate) (45 Mg) |
| Human | Pfizer Canada Ulc | 2013-08-21 | Cancelled Post Market | 2022-06-03 | Irinotecan | Irinotecan Hydrochloride (20 Mg) |
| Human | Pfizer Canada Ulc | 1998-08-11 | Cancelled Post Market | 2022-06-02 | Viracept 250 Mg | Nelfinavir (Nelfinavir Mesylate) (250 Mg) |
| Human | Pfizer Canada Ulc | 1997-07-04 | Cancelled Post Market | 2022-06-02 | Camptosar | Irinotecan Hydrochloride (20 Mg) |
| Human | Pfizer Canada Ulc | 2021-06-21 | Cancelled Pre Market | 2022-06-01 | Zoledronic Acid Injection A | Zoledronic Acid (Zoledronic Acid Monohydrate) (5 Mg) |
| Human | Pfizer Canada Ulc | 2003-03-21 | Cancelled Post Market | 2022-05-31 | Inderal La | Propranolol Hydrochloride (160 Mg) |
| Human | Pfizer Canada Ulc | 2003-03-21 | Cancelled Post Market | 2022-05-31 | Inderal La | Propranolol Hydrochloride (60 Mg) |
| Human | Pfizer Canada Ulc | 2003-03-21 | Cancelled Post Market | 2022-05-31 | Inderal La | Propranolol Hydrochloride (80 Mg) |
| Human | Pfizer Canada Ulc | 2003-03-21 | Cancelled Post Market | 2022-05-31 | Inderal La | Propranolol Hydrochloride (120 Mg) |
| Human | Pfizer Canada Ulc | 1998-03-19 | Marketed | 2022-05-20 | Depo Medrol With Lidocaine | Methylprednisolone Acetate (40 Mg)|Lidocaine Hydrochloride (10 Mg) |
| Human | Pfizer Canada Ulc | 2007-01-24 | Dormant | 2022-05-13 | Champix | Varenicline (Varenicline Tartrate) (0.5 Mg) |
| Human | Pfizer Canada Ulc | 2007-01-24 | Dormant | 2022-05-13 | Champix | Varenicline (Varenicline Tartrate) (1 Mg) |
| Human | Pfizer Canada Ulc | 2007-08-21 | Dormant | 2022-05-13 | Champix | Varenicline (Varenicline Tartrate) (0.5 Mg)|Varenicline (Varenicline Tartrate) (1 Mg) |
| Human | Pfizer Canada Ulc | 2013-03-06 | Cancelled Pre Market | 2022-04-29 | Ropivacaine Hydrochloride Injection Usp | Ropivacaine Hydrochloride (2 Mg) |
| Human | Pfizer Canada Ulc | 2021-12-20 | Marketed | 2022-04-25 | Depo Provera | Medroxyprogesterone Acetate (150 Mg) |
| Human | Pfizer Canada Ulc | 2005-07-07 | Cancelled Post Market | 2022-03-30 | Aricept Rdt | Donepezil Hydrochloride (5 Mg) |
Note: This table contains human, animal drugs, radiopharmaceutical and disinfectant regulated by CFIA(Canadian Food Inspection Agency) and Health Canada.
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "marketed" (case insensitive) to show drugs marketed.
Possible marketing statuses: Marketed, Approved, Dormant, Cancelled Pre Market, Cancelled Post Market, Cancelled (Safety Issue), Cancelled (Unreturned Annual).
⬤ any of (authorization/status change) date within 7 days.
⬤ any of (authorization/status change) date within 30 days.
⬤ any of (authorization/status change) date within 90 days.