Safety and effectiveness, and a substantial body of clinical evidence

Abbott's long-term investment in bioresorbable scaffold (BRS) technology and the dedication of the global clinical community combine to offer a substantial body of clinical evidence.

logo

ABSORB III met primary endpoint for FDA approval5

chart

Absorb met the primary endpoint of non-inferiority in the ABSORB III pivotal trial for FDA approval. The target lesion failure (TLF) rate at 1 year was 7.8% in the Absorb arm and 6.1% in the XIENCE arm. The Absorb arm was non-inferior to XIENCE (non-inferiority p-value of 0.0070).14

Comparable to XIENCE in ABSORB III5

chart

ABSORB III device thrombosis at 1 year

Appropriate vessel sizing—using Absorb in arteries with a reference vessel diameter (RVD) of ≥ 2.25 mm—revealed thrombosis rates similar to those with XIENCE.5

chart

pinch to zoom

Safety and effectiveness to 2 and 3 years

table

Outcomes at 2 years in early-use data sets show drug-eluting stent (DES)-like results for Absorb. A low accumulation of event rates has been seen in ABSORB EXTEND, even to 3 years.

Cohort B data at 5 years

This first-in-man, single-arm study of 101 patients may signal some unique Absorb benefits. Due to the limited number of clinical observations these results are only hypothesis generating; however they do set an encouraging precedent for the long-term results of ABSORB III and other ongoing trials.

Appearance of Vessel Treated with Absorb from ABSORB Cohort B18,19

Baseline Post-PCI5-Year Follow-up

NOTE: Visual depiction of the vessel is not necessarily indicative of normal functionality

Appearance of Untreated Human Vessel20

  • Restores* vessel functionality
  • Expands future treatment options
  • Avoids future complications—such as long-term stent fracture and strut malapposition—related to permanent metallic stents
  • Restores* vasomotor function

Lumen Gain Demonstrated in Serial IVUS Results13

chart

pinch to zoom

Vessel area is defined from center to external elastic lamina. Plaque area is defined from abluminal edge of scaffold struts to intimal surface. Lumen area is defined from center to endothelium. Full bioresorption occurs by approximately 3 years. There is significant reduction in plaque area (-0.89 mm2, p<0.01) and vessel area (-0.61 mm2, p=0.08) between 24 and 60 months.

Similarly, adverse cardiac events with Absorb were reduced at 5 years when compared with the best-in-class XIENCE stent.

Early Signals of Reduced Long-Term Events with Absorb13

chart

pinch to zoom

*Absorb improves coronary luminal diameter, restores blood flow and enables movement of the treated vessel. Source: Absorb GT1 IFU.

References

  • 1. Hernandez F. REPARA. EuroPCR. 2015.
  • 2. Hamm C. GABI-R. EuroPCR. 2015.
  • 3. Serruys P. TROFI II. ESC. 2015.
  • 4. De La Torre Hernandez JM et al. Presented at EuroPCR 2015.
  • 5. Kereiakes D. ABSORB III 1 Year. TCT. 2015.
  • 6. Kimura T et al. Eur Heart J. 2015;36:3332-3342. doi:10.1093/eurheartj/ehv435.
  • 7. Gao RL. ABSORB China 1 Year. TCT. 2015.
  • 8. Seth A. ABSORB FIRST. TCT. 2015.
  • 9. Capranzano P. GHOST-EU. EuroPCR. 2015.
  • 10. Chevalier BR. ABSORB II 2 Year. TCT. 2015.
  • 11. Schwencke C. ASSURE. TCT. 2015.
  • 12. Bartorelli A. ABSORB EXTEND. TCT. 2015.
  • 13. Serruys, P. ABSORB Cohort B, TCT 2015; early signals from Cohort B are under further evaluation in ABSORB III and ABSORB IV clinical trials.
  • 14. Ellis SG et al. N Engl J Med. 2015;373:1905-1915. doi: 10.1056/NEJMoa1509038.
  • 15 Wu CJ. ABSORB EXTEND. TCTAP. 2015.
  • 16. See Absorb GT1 FDA Panel Pack, March 2016, fda.gov.
  • 17. Stone GW. JAMA. 2008;299:1903-1913. doi:10.1001/jama.299.16.1903.
  • 18. Courtesy of Dr. R.J. van Geuns, Rotterdam, The Netherlands.
  • 19. De Bruyne B. ABSORB Cohort B 5 Year. TCT. 2014.
  • 20. Source: http://www.ptca.org/ivus/feldman.html

AP2942512-WBU Rev. A

Important Safety Information

Absorb GT1TM

Bioresorbable Vascular Scaffold System

INDICATIONS

The Absorb GT1 Bioresorbable Vascular Scaffold (BVS) is a temporary scaffold that will fully resorb over time and is indicated for improving coronary luminal diameter in patients with ischemic heart disease due to de novo native coronary artery lesions (length ≤ 24 mm) with a reference vessel diameter of ≥ 2.5 mm and ≤ 3.75 mm.

CONTRAINDICATIONS

The Absorb GT1 BVS System is contraindicated for use in:

  • Patients who cannot tolerate, including allergy or hypersensitivity to, procedural anticoagulation or the post-procedural antiplatelet regimen.
  • Patients with hypersensitivity or contraindication to everolimus or structurally‑related compounds, or known hypersensitivity to scaffold components (poly(L‑lactide), poly(D,L‑lactide), platinum) or with contrast sensitivity.

WARNINGS

  • For single use only. Do not resterilize or reuse. Note the product "Use by" date on the package.
  • Careful assessment of the target lesion reference vessel diameter and selection of the appropriate scaffold diameter relative to the target lesion reference vessel diameter are required to minimize potential damage to the scaffold during post-dilatation and to ensure adequate scaffold apposition and an appropriate post-implantation minimum lumen diameter.
  • In small vessels (visually assessed reference vessel diameter ≤ 2.75 mm), on-line QCA or intravascular imaging with intravascular ultrasound or optical coherence tomography is strongly recommended to accurately measure and confirm appropriate vessel sizing (reference vessel diameter ≥ 2.5 mm). (See Section 8.1.6 – Implantation of Absorb in Small Coronary Arteries (Post Hoc Analysis).)
  • If quantitative imaging determines a vessel size < 2.5 mm, do not implant the Absorb GT1 BVS. Implantation of the device in vessels < 2.5 mm may lead to an increased risk of adverse events such as myocardial infarction and scaffold thrombosis.
  • Adequate lesion preparation prior to scaffold implantation is required to ensure safe delivery of the scaffold across the target lesion. It is not recommended to treat patients having a lesion that prevents complete inflation of an angioplasty balloon. It is strongly recommended to achieve a residual stenosis between 20% and 40% after pre-dilatation to enable successful delivery and full expansion of the scaffold.
  • Ensure the scaffold is not post-dilated beyond the allowable expansion limits (see Absorb GT1 IFU Section 12.7 ‑ Clinician Use Information, Further Expansion of the Deployed Scaffold).
  • Antiplatelet therapy should be administered post-procedure (see Absorb GT1 IFU Section 9.1 ‑ Patient Selection and Treatment, Individualization of Treatment).
  • This product should not be used in patients who are not likely to comply with the recommended antiplatelet therapy.
  • Judicious selection of patients is necessary, since the use of this device carries the associated risk of scaffold thrombosis, vascular complications, and / or bleeding events.

PRECAUTIONS

  • Implantation of the scaffold should be performed only by physicians who have received appropriate training.
  • Do not exceed the Rated Burst Pressure (RBP) as indicated on the product label.
  • Post‑dilatation is strongly recommended for optimal scaffold apposition. When performed, post‑dilatation should be at high pressure (> 16 atm) with a noncompliant balloon.
  • Care must be taken to properly size the scaffold to ensure that the scaffold is in full contact with the arterial wall upon deflation of the balloon. All efforts should be made to ensure that the scaffold is not under dilated. Refer to Absorb GT1 IFU Section 12.7 - Clinical Use Information, Further Expansion of the Deployed Scaffold.
  • Balloon dilatation of any cells of a deployed Absorb GT1 BVS may cause scaffold damage. Avoid scaffolding across any side branches ≥ 2.0 mm in diameter. Placement of a scaffold has the potential to compromise side branch patency.
  • It is not recommended to treat patients having a lesion with excessive tortuosity proximal to or within the lesion.
  • Non‑clinical testing has demonstrated the Absorb GT1 BVS is MR Conditional. A patient with this device can be safely scanned in all MR environments 3T or less.
  • The safety and effectiveness of the Absorb GT1 BVS have not been established for subject populations with the following characteristics:
    • Coronary artery reference vessel diameters < 2.5 mm or > 3.75 mm
    • Lesion lengths > 24 mm
    • Lesions located in arterial or saphenous vein grafts
    • Lesions located in unprotected left main artery
    • Ostial lesions
    • Lesions located at a bifurcation
    • Previously stented lesions
    • Moderate to severe calcification
    • Chronic total occlusion or poor flow (< TIMI 1) distal to the identified lesions
    • Three‑vessel disease
    • Unresolved thrombus at the lesion site or anywhere in the vessel to be treated
    • Excessive tortuosity proximal to or within the lesion
    • Recent acute myocardial infarction (AMI)

POTENTIAL ADVERSE EVENTS

Adverse events that may be associated with PCI, treatment procedures and the use of a coronary scaffold in native coronary arteries include the following, but are not limited to:

  • Allergic reaction or hypersensitivity to latex, contrast agent, anesthesia, device materials (platinum, or polymer [poly(L‑lactide) (PLLA), polymer poly(D,L‑lactide) (PDLLA)]), and drug reactions to everolimus, anticoagulation, or antiplatelet drugs, Vascular access complications which may require transfusion or vessel repair, including: Catheter site reactions, Bleeding (ecchymosis, oozing, hematoma, hemorrhage, retroperitoneal hemorrhage), Arteriovenous fistula, pseudoaneurysm, aneurysm, dissection, perforation / rupture, Embolism (air, tissue, plaque, thrombotic material or device), Peripheral nerve injury, Peripheral ischemia, Coronary artery complications which may require additional intervention, including: Total occlusion or abrupt closure, Arteriovenous fistula, pseudoaneurysm, aneurysm, dissection, perforation / rupture, Tissue prolapse / plaque shift, Embolism (air, tissue, plaque, thrombotic material or device), Coronary or scaffold thrombosis (acute, subacute, late, very late), Stenosis or restenosis, Pericardial complications which may require additional intervention, including: Cardiac tamponade, Pericardial effusion, Pericarditis, Cardiac arrhythmias (including conduction disorders, atrial and ventricular arrhythmias), Cardiac ischemic conditions (including myocardial ischemia, myocardial infarction [including acute], coronary artery spasm and unstable or stable angina pectoris), Stroke / Cerebrovascular accident (CVA) and Transient Ischemic Attack (TIA), System organ failures: Cardio‑respiratory arrest, Cardiac failure, Cardiopulmonary failure (including pulmonary edema), Renal insufficiency / failure, Shock, Blood cell disorders (including Heparin Induced Thrombocytopenia [HIT]), Hypotension / hypertension, Infection, Nausea and vomiting, Palpitations, dizziness, and syncope, Chest pain, Fever, Pain, Death.