Experienced spine and sports medicine physician of 18 years. Master diagnostician of musculoskeletal and other pain disorders with prevention and rehabilitation focused approach to injury and disease. Experience with industrial injuries, return to work documentation and legal records review. Focused on whole person approach to healing using functional medicine principles in addition to traditional medical model of care.
Provide interventional and conservative sports and spine care including thorough diagnostic workup, imaging interpretation, spinal interventions, medical pain management, functional medicine testing and personalized wellness plans and preventive musculoskeletal care.
I serve as a medical expert alongside other physicians on the medical panel to assist the judge in resolving disputed worker's compensation claims. I review medical records and render independent opinions on causality and necessary medical care as well as future care considerations. Patient interviews and exams are conducted virtually.
Independent contractor providing remote and in-person medical services relating to musculoskeletal medicine, spine care, pain management, industrial medicine, functional medicine, physical medicine and rehabilitation, clinical research and medical-legal expert services
2013: A Prospective, Randomized, Controlled Pivotal Clinical Investigation of the XXXX® Spinal Stabilization System in Patients with Lumbar Degenerative Disc Disease
2013: A Pivotal, Multi-Center, Double-Blind Study of the Safety and Effectiveness of XXX (XX) in Patients with Mild to Moderate Osteoarthritis of the Hip
2012-2013: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy And Safety Of XXX In Subjects With Neuropathic Pain From Lumbosacral Radiculopathy
2013: A Multicenter, Randomized, Double-blind, Controlled, Comparative Study of
XXX in Patients with Lumbar Disc Herniation (Phase III)
2014: A Randomized, Double-blind, Placebo-controlled, Multi-dose Phase 2 Study Evaluating the Safety and Efficacy of Intra-articular Injections of XXX in Subjects with Mild to Moderate Patello-Femoral Osteoarthritis Involving Both Knees
2015: A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to
Evaluate the Efficacy and Safety of XXX in Patients with Pain due to Osteoarthritis of the Knee or Hip
2015: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Discogenic Lumbar Back Pain Through 12 Months
Amended to: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Low Back Pain
2015: A Multicenter, Open-label study of XXX in Patients with Lumbar Disc Herniation (Phase III) Protocol number: 6603-1132 (217079)
2015-16: A Multicenter, Non-Treatment, Follow-up Study to Assess the Health Economic Outcomes of Previous Pulsed Electromagnetic Field (PEMF) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery #RBI.2015.001B
2016: A Phase 3, Randomized, Double Blind, Placebo And Active Controlled, Multicenter, Parallel Group Study Of The Analgesic Efficacy And Safety Of XXX In Adult Subjects With Chronic Low Back Pain #A4091059
2016 HS-16-555: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Enriched-Enrollment Withdrawal, Multicenter Study to Evaluate the Efficacy and Safety of a Long-Acting Subcutaneous Injectable Depot of XXX (XX) in Subjects with a Recent History of Moderate to Severe Chronic Low Back Pain Currently Treated with Opioids
2018: TO START: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and Lawrence Grade 2 or 3 Osteoarthritis of the Knee
2018: DGX-A01: A Prospective, Randomized, Double-Blinded, Vehicle-and Placebo-Controlled, Multicenter Study to Evaluate the Safety and Preliminary Efficacy of XXX in Subjects with Single-Level, Symptomatic Lumbar Intervertebral Disc Degeneration
2019: SM04690-OA-11 A Phase 3, 56-Week, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study Utilizing Patient Reported and Radiographic Outcomes to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2019: Corticosteroid Lumbar Epidural Analgesia for Radiculopathy (C.L.E.A.R.)
2019- SM04690-OA-10 A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind,
Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2020-SM04690-OA-07 A 48-Week, Placebo-Controlled, Single Blind Extension Study
Evaluating the Safety and Efficacy of XXX in Subjects with Osteoarthritis of the Knee
2020 - A Phase 3, 14-Day, Double-blind, Randomized, Placebo-Controlled, Multicenter
Study of the Efficacy and Safety of XXX 100 mg and 200 mg TID in Subjects with Pain Due to Acute Back Muscle Spasm
2020 to- An Open-Label, Single Ascending Dose Study to Assess the Safety and
Tolerability of XXX in Patients with Osteoarthritis of the Knee
2019-2022 A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-
Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of 3 Doses of XXX as
Compared to Placebo After 12 Weeks of Treatment in Patients with Treatment-Resistant
Hypertension (rHTN)
2022: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-
Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and
Lawrence Grade 2 or 3 Osteoarthritis of the Knee (previously on hold since 2018)
2022: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group,
Multicenter Study to Evaluate the Safety and Efficacy of XXX in Subjects with
Moderate to Severe Acute Lower Back Pain
2022: RTX-OAK-201 A Phase 2, Randomized, Active and Placebo-Controlled,
Dose-Ranging Study to Evaluate the Efficacy and Safety of Intra-Articular XXXX to
Treat Moderate to Severe Pain from Knee Osteoarthritis (RTX-OAK-201)
2023: as PI: Sciatica Epidural Radiculopathy Experimental New Interventional
TherapY Clonidine Micropellet
2024: Start as Sub-I: Protocol I8F-MC-GPGN(a) The Effect of XXXXX versus XXXXX on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes (SURPASS-CVOT) Angela Krull, MD/Study Listing (04/16/2024)
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind Study to Investigate the
Efficacy and Safety of Once- Daily Oral XXXXX Compared with Placebo in Adult
Participants with Obesity or Overweight with Weight-Related Comorbidities (ATTAIN-1). Protocol: J2A-MC-GZGP
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind, Parallel-Group, Event- Driven, Cardiovascular Safety Study with BI XXXXX Administered Subcutaneously Compared with Placebo in Participants with Overweight or Obesity with Established Cardiovascular Disease (CVD) or Chronic Kidney Disease, And/or at Least Two Weight- Related Complications or Risk Factors for CVD.
2024: Start as PI: A Randomized, Double-Blind, Single Ascending Dose Phase 1 Study of XXXX Intra-Articular Injection for Subjects with Mild to Moderate Osteoarthritis of the Knee
2024: Start as PI: A Phase 3, Multicenter, Randomized, Double-blind, Single-dose Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Glenohumeral OsteoarthritisPfizer
2013: A Prospective, Randomized, Controlled Pivotal Clinical Investigation of the XXXX® Spinal Stabilization System in Patients with Lumbar Degenerative Disc Disease
2013: A Pivotal, Multi-Center, Double-Blind Study of the Safety and Effectiveness of XXX (XX) in Patients with Mild to Moderate Osteoarthritis of the Hip
2012-2013: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy And Safety Of XXX In Subjects With Neuropathic Pain From Lumbosacral Radiculopathy
2013: A Multicenter, Randomized, Double-blind, Controlled, Comparative Study of
XXX in Patients with Lumbar Disc Herniation (Phase III)
2014: A Randomized, Double-blind, Placebo-controlled, Multi-dose Phase 2 Study Evaluating the Safety and Efficacy of Intra-articular Injections of XXX in Subjects with Mild to Moderate Patello-Femoral Osteoarthritis Involving Both Knees
2015: A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to
Evaluate the Efficacy and Safety of XXX in Patients with Pain due to Osteoarthritis of the Knee or Hip
2015: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Discogenic Lumbar Back Pain Through 12 Months
Amended to: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Low Back Pain
2015: A Multicenter, Open-label study of XXX in Patients with Lumbar Disc Herniation (Phase III) Protocol number: 6603-1132 (217079)
2015-16: A Multicenter, Non-Treatment, Follow-up Study to Assess the Health Economic Outcomes of Previous Pulsed Electromagnetic Field (PEMF) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery #RBI.2015.001B
2016: A Phase 3, Randomized, Double Blind, Placebo And Active Controlled, Multicenter, Parallel Group Study Of The Analgesic Efficacy And Safety Of XXX In Adult Subjects With Chronic Low Back Pain #A4091059
2016 HS-16-555: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Enriched-Enrollment Withdrawal, Multicenter Study to Evaluate the Efficacy and Safety of a Long-Acting Subcutaneous Injectable Depot of XXX (XX) in Subjects with a Recent History of Moderate to Severe Chronic Low Back Pain Currently Treated with Opioids
2018: TO START: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and Lawrence Grade 2 or 3 Osteoarthritis of the Knee
2018: DGX-A01: A Prospective, Randomized, Double-Blinded, Vehicle-and Placebo-Controlled, Multicenter Study to Evaluate the Safety and Preliminary Efficacy of XXX in Subjects with Single-Level, Symptomatic Lumbar Intervertebral Disc Degeneration
2019: SM04690-OA-11 A Phase 3, 56-Week, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study Utilizing Patient Reported and Radiographic Outcomes to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2019: Corticosteroid Lumbar Epidural Analgesia for Radiculopathy (C.L.E.A.R.)
2019- SM04690-OA-10 A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind,
Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2020-SM04690-OA-07 A 48-Week, Placebo-Controlled, Single Blind Extension Study
Evaluating the Safety and Efficacy of XXX in Subjects with Osteoarthritis of the Knee
2020 - A Phase 3, 14-Day, Double-blind, Randomized, Placebo-Controlled, Multicenter
Study of the Efficacy and Safety of XXX 100 mg and 200 mg TID in Subjects with Pain Due to Acute Back Muscle Spasm
2020 to- An Open-Label, Single Ascending Dose Study to Assess the Safety and
Tolerability of XXX in Patients with Osteoarthritis of the Knee
2019-2022 A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-
Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of 3 Doses of XXX as
Compared to Placebo After 12 Weeks of Treatment in Patients with Treatment-Resistant
Hypertension (rHTN)
2022: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-
Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and
Lawrence Grade 2 or 3 Osteoarthritis of the Knee (previously on hold since 2018)
2022: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group,
Multicenter Study to Evaluate the Safety and Efficacy of XXX in Subjects with
Moderate to Severe Acute Lower Back Pain
2022: RTX-OAK-201 A Phase 2, Randomized, Active and Placebo-Controlled,
Dose-Ranging Study to Evaluate the Efficacy and Safety of Intra-Articular XXXX to
Treat Moderate to Severe Pain from Knee Osteoarthritis (RTX-OAK-201)
2023: as PI: Sciatica Epidural Radiculopathy Experimental New Interventional
TherapY Clonidine Micropellet
2024: Start as Sub-I: Protocol I8F-MC-GPGN(a) The Effect of XXXXX versus XXXXX on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes (SURPASS-CVOT) Angela Krull, MD/Study Listing (04/16/2024)
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind Study to Investigate the
Efficacy and Safety of Once- Daily Oral XXXXX Compared with Placebo in Adult
Participants with Obesity or Overweight with Weight-Related Comorbidities (ATTAIN-1). Protocol: J2A-MC-GZGP
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind, Parallel-Group, Event- Driven, Cardiovascular Safety Study with BI XXXXX Administered Subcutaneously Compared with Placebo in Participants with Overweight or Obesity with Established Cardiovascular Disease (CVD) or Chronic Kidney Disease, And/or at Least Two Weight- Related Complications or Risk Factors for CVD.
2024: Start as PI: A Randomized, Double-Blind, Single Ascending Dose Phase 1 Study of XXXX Intra-Articular Injection for Subjects with Mild to Moderate Osteoarthritis of the Knee
2024: Start as PI: A Phase 3, Multicenter, Randomized, Double-blind, Single-dose Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Glenohumeral OsteoarthritisPfizer
2013: A Prospective, Randomized, Controlled Pivotal Clinical Investigation of the XXXX® Spinal Stabilization System in Patients with Lumbar Degenerative Disc Disease
2013: A Pivotal, Multi-Center, Double-Blind Study of the Safety and Effectiveness of XXX (XX) in Patients with Mild to Moderate Osteoarthritis of the Hip
2012-2013: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy And Safety Of XXX In Subjects With Neuropathic Pain From Lumbosacral Radiculopathy
2013: A Multicenter, Randomized, Double-blind, Controlled, Comparative Study of
XXX in Patients with Lumbar Disc Herniation (Phase III)
2014: A Randomized, Double-blind, Placebo-controlled, Multi-dose Phase 2 Study Evaluating the Safety and Efficacy of Intra-articular Injections of XXX in Subjects with Mild to Moderate Patello-Femoral Osteoarthritis Involving Both Knees
2015: A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to
Evaluate the Efficacy and Safety of XXX in Patients with Pain due to Osteoarthritis of the Knee or Hip
2015: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Discogenic Lumbar Back Pain Through 12 Months
Amended to: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Low Back Pain
2015: A Multicenter, Open-label study of XXX in Patients with Lumbar Disc Herniation (Phase III) Protocol number: 6603-1132 (217079)
2015-16: A Multicenter, Non-Treatment, Follow-up Study to Assess the Health Economic Outcomes of Previous Pulsed Electromagnetic Field (PEMF) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery #RBI.2015.001B
2016: A Phase 3, Randomized, Double Blind, Placebo And Active Controlled, Multicenter, Parallel Group Study Of The Analgesic Efficacy And Safety Of XXX In Adult Subjects With Chronic Low Back Pain #A4091059
2016 HS-16-555: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Enriched-Enrollment Withdrawal, Multicenter Study to Evaluate the Efficacy and Safety of a Long-Acting Subcutaneous Injectable Depot of XXX (XX) in Subjects with a Recent History of Moderate to Severe Chronic Low Back Pain Currently Treated with Opioids
2018: TO START: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and Lawrence Grade 2 or 3 Osteoarthritis of the Knee
2018: DGX-A01: A Prospective, Randomized, Double-Blinded, Vehicle-and Placebo-Controlled, Multicenter Study to Evaluate the Safety and Preliminary Efficacy of XXX in Subjects with Single-Level, Symptomatic Lumbar Intervertebral Disc Degeneration
2019: SM04690-OA-11 A Phase 3, 56-Week, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study Utilizing Patient Reported and Radiographic Outcomes to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2019: Corticosteroid Lumbar Epidural Analgesia for Radiculopathy (C.L.E.A.R.)
2019- SM04690-OA-10 A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind,
Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2020-SM04690-OA-07 A 48-Week, Placebo-Controlled, Single Blind Extension Study
Evaluating the Safety and Efficacy of XXX in Subjects with Osteoarthritis of the Knee
2020 - A Phase 3, 14-Day, Double-blind, Randomized, Placebo-Controlled, Multicenter
Study of the Efficacy and Safety of XXX 100 mg and 200 mg TID in Subjects with Pain Due to Acute Back Muscle Spasm
2020 to- An Open-Label, Single Ascending Dose Study to Assess the Safety and
Tolerability of XXX in Patients with Osteoarthritis of the Knee
2019-2022 A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-
Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of 3 Doses of XXX as
Compared to Placebo After 12 Weeks of Treatment in Patients with Treatment-Resistant
Hypertension (rHTN)
2022: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-
Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and
Lawrence Grade 2 or 3 Osteoarthritis of the Knee (previously on hold since 2018)
2022: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group,
Multicenter Study to Evaluate the Safety and Efficacy of XXX in Subjects with
Moderate to Severe Acute Lower Back Pain
2022: RTX-OAK-201 A Phase 2, Randomized, Active and Placebo-Controlled,
Dose-Ranging Study to Evaluate the Efficacy and Safety of Intra-Articular XXXX to
Treat Moderate to Severe Pain from Knee Osteoarthritis (RTX-OAK-201)
2023: as PI: Sciatica Epidural Radiculopathy Experimental New Interventional
TherapY Clonidine Micropellet
2024: Start as Sub-I: Protocol I8F-MC-GPGN(a) The Effect of XXXXX versus XXXXX on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes (SURPASS-CVOT) Angela Krull, MD/Study Listing (04/16/2024)
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind Study to Investigate the
Efficacy and Safety of Once- Daily Oral XXXXX Compared with Placebo in Adult
Participants with Obesity or Overweight with Weight-Related Comorbidities (ATTAIN-1). Protocol: J2A-MC-GZGP
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind, Parallel-Group, Event- Driven, Cardiovascular Safety Study with BI XXXXX Administered Subcutaneously Compared with Placebo in Participants with Overweight or Obesity with Established Cardiovascular Disease (CVD) or Chronic Kidney Disease, And/or at Least Two Weight- Related Complications or Risk Factors for CVD.
2024: Start as PI: A Randomized, Double-Blind, Single Ascending Dose Phase 1 Study of XXXX Intra-Articular Injection for Subjects with Mild to Moderate Osteoarthritis of the Knee
2024: Start as PI: A Phase 3, Multicenter, Randomized, Double-blind, Single-dose Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Glenohumeral OsteoarthritisPfizer
2013: A Prospective, Randomized, Controlled Pivotal Clinical Investigation of the XXXX® Spinal Stabilization System in Patients with Lumbar Degenerative Disc Disease
2013: A Pivotal, Multi-Center, Double-Blind Study of the Safety and Effectiveness of XXX (XX) in Patients with Mild to Moderate Osteoarthritis of the Hip
2012-2013: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study To Evaluate The Efficacy And Safety Of XXX In Subjects With Neuropathic Pain From Lumbosacral Radiculopathy
2013: A Multicenter, Randomized, Double-blind, Controlled, Comparative Study of
XXX in Patients with Lumbar Disc Herniation (Phase III)
2014: A Randomized, Double-blind, Placebo-controlled, Multi-dose Phase 2 Study Evaluating the Safety and Efficacy of Intra-articular Injections of XXX in Subjects with Mild to Moderate Patello-Femoral Osteoarthritis Involving Both Knees
2015: A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to
Evaluate the Efficacy and Safety of XXX in Patients with Pain due to Osteoarthritis of the Knee or Hip
2015: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Discogenic Lumbar Back Pain Through 12 Months
Amended to: MSB-DR003: A Prospective, Multicenter, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Alone or Combined with Hyaluronic Acid (HA) in Subjects with Chronic Low Back Pain
2015: A Multicenter, Open-label study of XXX in Patients with Lumbar Disc Herniation (Phase III) Protocol number: 6603-1132 (217079)
2015-16: A Multicenter, Non-Treatment, Follow-up Study to Assess the Health Economic Outcomes of Previous Pulsed Electromagnetic Field (PEMF) Therapy in the Treatment of Persistent Post-Operative Pain Following Lumbar Surgery #RBI.2015.001B
2016: A Phase 3, Randomized, Double Blind, Placebo And Active Controlled, Multicenter, Parallel Group Study Of The Analgesic Efficacy And Safety Of XXX In Adult Subjects With Chronic Low Back Pain #A4091059
2016 HS-16-555: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Enriched-Enrollment Withdrawal, Multicenter Study to Evaluate the Efficacy and Safety of a Long-Acting Subcutaneous Injectable Depot of XXX (XX) in Subjects with a Recent History of Moderate to Severe Chronic Low Back Pain Currently Treated with Opioids
2018: TO START: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and Lawrence Grade 2 or 3 Osteoarthritis of the Knee
2018: DGX-A01: A Prospective, Randomized, Double-Blinded, Vehicle-and Placebo-Controlled, Multicenter Study to Evaluate the Safety and Preliminary Efficacy of XXX in Subjects with Single-Level, Symptomatic Lumbar Intervertebral Disc Degeneration
2019: SM04690-OA-11 A Phase 3, 56-Week, Multicenter, Randomized, Double-Blind, Vehicle-Controlled Study Utilizing Patient Reported and Radiographic Outcomes to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2019: Corticosteroid Lumbar Epidural Analgesia for Radiculopathy (C.L.E.A.R.)
2019- SM04690-OA-10 A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind,
Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
2020-SM04690-OA-07 A 48-Week, Placebo-Controlled, Single Blind Extension Study
Evaluating the Safety and Efficacy of XXX in Subjects with Osteoarthritis of the Knee
2020 - A Phase 3, 14-Day, Double-blind, Randomized, Placebo-Controlled, Multicenter
Study of the Efficacy and Safety of XXX 100 mg and 200 mg TID in Subjects with Pain Due to Acute Back Muscle Spasm
2020 to- An Open-Label, Single Ascending Dose Study to Assess the Safety and
Tolerability of XXX in Patients with Osteoarthritis of the Knee
2019-2022 A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-
Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of 3 Doses of XXX as
Compared to Placebo After 12 Weeks of Treatment in Patients with Treatment-Resistant
Hypertension (rHTN)
2022: Protocol TGC12301: A Randomized, Double-Blind, Placebo-Controlled, Multi-
Center, Phase 3 Study to Determine the Efficacy of XXX in Subjects with Kellgren and
Lawrence Grade 2 or 3 Osteoarthritis of the Knee (previously on hold since 2018)
2022: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group,
Multicenter Study to Evaluate the Safety and Efficacy of XXX in Subjects with
Moderate to Severe Acute Lower Back Pain
2022: RTX-OAK-201 A Phase 2, Randomized, Active and Placebo-Controlled,
Dose-Ranging Study to Evaluate the Efficacy and Safety of Intra-Articular XXXX to
Treat Moderate to Severe Pain from Knee Osteoarthritis (RTX-OAK-201)
2023: as PI: Sciatica Epidural Radiculopathy Experimental New Interventional
TherapY Clonidine Micropellet
2024: Start as Sub-I: Protocol I8F-MC-GPGN(a) The Effect of XXXXX versus XXXXX on Major Adverse Cardiovascular Events in Patients with Type 2 Diabetes (SURPASS-CVOT) Angela Krull, MD/Study Listing (04/16/2024)
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind Study to Investigate the
Efficacy and Safety of Once- Daily Oral XXXXX Compared with Placebo in Adult
Participants with Obesity or Overweight with Weight-Related Comorbidities (ATTAIN-1). Protocol: J2A-MC-GZGP
2024: Start as Sub-I: A Phase 3, Randomized, Double-Blind, Parallel-Group, Event- Driven, Cardiovascular Safety Study with BI XXXXX Administered Subcutaneously Compared with Placebo in Participants with Overweight or Obesity with Established Cardiovascular Disease (CVD) or Chronic Kidney Disease, And/or at Least Two Weight- Related Complications or Risk Factors for CVD.
2024: Start as PI: A Randomized, Double-Blind, Single Ascending Dose Phase 1 Study of XXXX Intra-Articular Injection for Subjects with Mild to Moderate Osteoarthritis of the Knee
2024: Start as PI: A Phase 3, Multicenter, Randomized, Double-blind, Single-dose Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Glenohumeral OsteoarthritisPfizer